Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HE13
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.708 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.697 |
CLV_Separin_Metazoa | 61 | 65 | PF03568 | 0.319 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.483 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.416 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.422 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.455 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.639 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.484 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.417 |
LIG_Actin_WH2_2 | 143 | 160 | PF00022 | 0.307 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.423 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.296 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.439 |
LIG_LIR_Apic_2 | 276 | 280 | PF02991 | 0.770 |
LIG_LIR_Apic_2 | 303 | 307 | PF02991 | 0.670 |
LIG_LIR_Gen_1 | 74 | 82 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.290 |
LIG_PTB_Apo_2 | 113 | 120 | PF02174 | 0.404 |
LIG_Rb_LxCxE_1 | 21 | 35 | PF01857 | 0.303 |
LIG_SH2_CRK | 277 | 281 | PF00017 | 0.848 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.660 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.295 |
LIG_SH2_GRB2like | 295 | 298 | PF00017 | 0.794 |
LIG_SH2_GRB2like | 331 | 334 | PF00017 | 0.659 |
LIG_SH2_NCK_1 | 304 | 308 | PF00017 | 0.663 |
LIG_SH2_NCK_1 | 319 | 323 | PF00017 | 0.630 |
LIG_SH2_SRC | 331 | 334 | PF00017 | 0.740 |
LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.652 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.637 |
LIG_SH2_STAT3 | 241 | 244 | PF00017 | 0.625 |
LIG_SH2_STAT3 | 246 | 249 | PF00017 | 0.641 |
LIG_SH2_STAT3 | 251 | 254 | PF00017 | 0.739 |
LIG_SH2_STAT3 | 33 | 36 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.290 |
LIG_SUMO_SIM_anti_2 | 20 | 28 | PF11976 | 0.401 |
LIG_UBA3_1 | 26 | 34 | PF00899 | 0.296 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.295 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.386 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.682 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.423 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.402 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.441 |
MOD_Cter_Amidation | 216 | 219 | PF01082 | 0.453 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.747 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.655 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.412 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.567 |
MOD_GlcNHglycan | 325 | 329 | PF01048 | 0.506 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.736 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.565 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.333 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.425 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.567 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.507 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.565 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.465 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.454 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.430 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.412 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.454 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.293 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.399 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.362 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.330 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.312 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.506 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.391 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.428 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.464 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.703 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.414 |
MOD_SUMO_rev_2 | 128 | 134 | PF00179 | 0.406 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.290 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.727 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IN96 | Leishmania donovani | 53% | 100% |
A4I1C0 | Leishmania infantum | 54% | 100% |
E9AXF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
Q4QA16 | Leishmania major | 57% | 99% |