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UniProt P12499

P12499

P12499 (UniProt P12499): 30 experimental structures on GenesisL1. Binding sites, pockets, druggability and 3D structures in GL1X.

UniProt
P12499
Experimental structures
30
Predicted models
0

Structures

30 records of P12499 in the MolNFT archive: 30 experimental, 0 predicted.

EntryTitleMethodChainsLigandsPockets
1E28Nonstandard peptide binding of HLA-B*5101 complexed with HIV immunodominant epitope KM2(TAFTIPSI)x-ray diffractionC——
1E28Nonstandard peptide binding of HLA-B*5101 complexed with HIV immunodominant epitope KM2(TAFTIPSI)x-ray diffractionC——
1HXWHIV-1 protease dimer complexed with a-84538x-ray diffractionA, B——
1HXWHIV-1 protease dimer complexed with a-84538x-ray diffractionA, B——
1P7QCrystal Structure of HLA-A2 Bound to LIR-1, a Host and Viral MHC Receptorx-ray diffractionC——
1P7QCrystal structure of HLA-A2 bound to lir-1, a host and viral MHC receptorx-ray diffractionC——
1PROHIV-1 protease dimer complexed with a-98881x-ray diffractionA, B——
1PROHIV-1 protease dimer complexed with a-98881x-ray diffractionA, B——
1Q94Structures of HLA-A*1101 in complex with immunodominant nonamer and decamer HIV-1 epitopes clearly…x-ray diffractionC, F——
1Q94Structures of HLA-A*1101 in complex with immunodominant nonamer and decamer HIV-1 epitopes clearly…x-ray diffractionC, F——
1VIJHIV-1 protease complexed with the inhibitor HOE/BAY 793 hexagonal formx-ray diffractionA, B——
1VIJHIV-1 protease complexed with the inhibitor HOE/BAY 793 hexagonal formx-ray diffractionA, B——
1VIKHIV-1 protease complexed with the inhibitor HOE/BAY 793 orthorhombic formx-ray diffractionA, B——
1VIKHIV-1 protease complexed with the inhibitor HOE/BAY 793 orthorhombic formx-ray diffractionA, B——
3W39Crystal structure of HLA-B*5201 in complexed with HIV immunodominant epitope (TAFTIPSI)x-ray diffractionC, F——
3W39Crystal structure of HLA-B*5201 in complexed with HIV immunodominant epitope (taftipsi)x-ray diffractionC, F——
4EJ8Apo HIV Protease (PR) dimer in closed form with fragment 1F1 in the outside/top of flapx-ray diffractionA, B——
4EJ8Apo HIV protease (pr) dimer in closed form with fragment 1F1 in the OUTSIDE/TOP of flapx-ray diffractionA, B——
4EJDHIV Protease (PR) dimer in closed form with pepstatin in active site and fragment 1F1 in the…x-ray diffractionA, B——
4EJDHIV protease (pr) dimer in closed form with pepstatin in active site and fragment 1F1 in the…x-ray diffractionA, B——
4EJKHIV Protease (PR) dimer in closed form with pepstatin in active site and fragment 1F1-N in the…x-ray diffractionA, B——
4EJKHIV protease (pr) dimer in closed form with pepstatin in active site and fragment 1F1-N in the…x-ray diffractionA, B——
4EJLApo HIV Protease (PR) dimer in closed form with fragment 1F1-N in the outside/top of flapx-ray diffractionA, B——
4EJLApo HIV protease (pr) dimer in closed form with fragment 1F1-N in the OUTSIDE/TOP of flapx-ray diffractionA, B——
4K4PTL-3 inhibited Trp6Ala HIV Proteasex-ray diffractionA, B——
4K4PTl-3 inhibited TRP6ALA HIV proteasex-ray diffractionA, B——
4K4QTL-3 inhibited Trp6Ala HIV Protease with 3-bromo-2,6-dimethoxybenzoic acid bound in flap sitex-ray diffractionA, B——
4K4QTl-3 inhibited TRP6ALA HIV protease with 3-bromo-2,6-dimethoxybenzoic acid bound in flap sitex-ray diffractionA, B——
4K4RTL-3 inhibited Trp6Ala HIV Protease with 1-bromo-2-napthoic acid bound in exositex-ray diffractionA, B——
4K4RTl-3 inhibited TRP6ALA HIV protease with 1-bromo-2-napthoic acid bound in exositex-ray diffractionA, B——

Elsewhere

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