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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 20 |
GO:0042995 | cell projection | 2 | 20 |
GO:0043226 | organelle | 2 | 20 |
GO:0043227 | membrane-bounded organelle | 3 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 20 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 20 |
GO:0005743 | mitochondrial inner membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 2 |
GO:0019866 | organelle inner membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
Related structures:
AlphaFold database: A4H7G0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.533 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.503 |
CLV_Separin_Metazoa | 407 | 411 | PF03568 | 0.281 |
DEG_APCC_DBOX_1 | 134 | 142 | PF00400 | 0.275 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.539 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.592 |
DOC_CDC14_PxL_1 | 199 | 207 | PF14671 | 0.359 |
DOC_CDC14_PxL_1 | 333 | 341 | PF14671 | 0.417 |
DOC_CDC14_PxL_1 | 378 | 386 | PF14671 | 0.309 |
DOC_CDC14_PxL_1 | 423 | 431 | PF14671 | 0.483 |
DOC_CYCLIN_RxL_1 | 278 | 286 | PF00134 | 0.323 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 46 | 55 | PF00134 | 0.366 |
DOC_CYCLIN_yCln2_LP_2 | 442 | 448 | PF00134 | 0.255 |
DOC_MAPK_DCC_7 | 198 | 207 | PF00069 | 0.228 |
DOC_MAPK_gen_1 | 120 | 128 | PF00069 | 0.445 |
DOC_MAPK_HePTP_8 | 69 | 81 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 112 | 119 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 139 | 147 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 198 | 207 | PF00069 | 0.228 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.500 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 198 | 206 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 22 | 27 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 241 | 249 | PF00244 | 0.264 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 370 | 378 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.578 |
LIG_Actin_WH2_2 | 122 | 137 | PF00022 | 0.264 |
LIG_Actin_WH2_2 | 326 | 342 | PF00022 | 0.467 |
LIG_Actin_WH2_2 | 36 | 54 | PF00022 | 0.543 |
LIG_APCC_ABBA_1 | 156 | 161 | PF00400 | 0.244 |
LIG_APCC_ABBAyCdc20_2 | 61 | 67 | PF00400 | 0.286 |
LIG_BRCT_BRCA1_1 | 173 | 177 | PF00533 | 0.243 |
LIG_DLG_GKlike_1 | 139 | 146 | PF00625 | 0.327 |
LIG_DLG_GKlike_1 | 281 | 288 | PF00625 | 0.303 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.535 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.495 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.415 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.443 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.297 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.504 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.369 |
LIG_Integrin_RGD_1 | 120 | 122 | PF01839 | 0.349 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 388 | 397 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.465 |
LIG_NRBOX | 76 | 82 | PF00104 | 0.338 |
LIG_SUMO_SIM_anti_2 | 124 | 132 | PF11976 | 0.511 |
LIG_SUMO_SIM_anti_2 | 142 | 147 | PF11976 | 0.567 |
LIG_SUMO_SIM_anti_2 | 257 | 263 | PF11976 | 0.285 |
LIG_SUMO_SIM_anti_2 | 273 | 278 | PF11976 | 0.530 |
LIG_SUMO_SIM_anti_2 | 405 | 410 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 204 | 209 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 281 | 286 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 295 | 300 | PF11976 | 0.458 |
LIG_TRAF2_2 | 228 | 233 | PF00917 | 0.437 |
LIG_UBA3_1 | 442 | 451 | PF00899 | 0.412 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.405 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.517 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.498 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.448 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.232 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.350 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.316 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.335 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.337 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.509 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.513 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.247 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.380 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.350 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.419 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.346 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.358 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.323 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.653 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.434 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.480 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.242 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.351 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.515 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.346 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.549 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.450 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.542 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.606 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.574 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.623 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.449 |
MOD_OFUCOSY | 92 | 99 | PF10250 | 0.338 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.475 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.333 |
MOD_PK_1 | 295 | 301 | PF00069 | 0.303 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.478 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.571 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.431 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.473 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.648 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.469 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.464 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.408 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.435 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.557 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.346 |
MOD_Plk_2-3 | 317 | 323 | PF00069 | 0.289 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.547 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.383 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.470 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.215 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.376 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.383 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.485 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.430 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.522 |
TRG_DiLeu_BaEn_1 | 36 | 41 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 27 | 32 | PF01217 | 0.570 |
TRG_DiLeu_BaLyEn_6 | 278 | 283 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 75 | 80 | PF01217 | 0.459 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.311 |
TRG_ER_diArg_1 | 382 | 385 | PF00400 | 0.313 |
TRG_NES_CRM1_1 | 201 | 211 | PF08389 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 78 | 82 | PF00026 | 0.470 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F9 | Leptomonas seymouri | 33% | 88% |
A0A0N0P8N9 | Leptomonas seymouri | 32% | 70% |
A0A0N1HZK9 | Leptomonas seymouri | 31% | 87% |
A0A0N1I0W0 | Leptomonas seymouri | 30% | 90% |
A0A0N1I1E8 | Leptomonas seymouri | 26% | 100% |
A0A1X0NEN5 | Trypanosomatidae | 25% | 79% |
A0A1X0NG16 | Trypanosomatidae | 27% | 79% |
A0A1X0P4M6 | Trypanosomatidae | 25% | 79% |
A0A3Q8I8N4 | Leishmania donovani | 77% | 100% |
A0A3S5H5M6 | Leishmania donovani | 23% | 86% |
A4H3R1 | Leishmania braziliensis | 29% | 67% |
A4H4H0 | Leishmania braziliensis | 23% | 100% |
A4HSP5 | Leishmania infantum | 23% | 86% |
E9AGK6 | Leishmania infantum | 77% | 100% |
E9AKN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9APJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QFY4 | Leishmania major | 78% | 100% |
V5BMQ2 | Trypanosoma cruzi | 26% | 82% |