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. | yes | yes: 10 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0101031 | protein folding chaperone complex | 3 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: E9ACV9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.664 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.501 |
CLV_PCSK_FUR_1 | 299 | 303 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.448 |
DEG_APCC_DBOX_1 | 16 | 24 | PF00400 | 0.593 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.287 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.268 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.566 |
DEG_SCF_FBW7_1 | 333 | 340 | PF00400 | 0.537 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.633 |
DEG_SPOP_SBC_1 | 338 | 342 | PF00917 | 0.725 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.770 |
DOC_CKS1_1 | 472 | 477 | PF01111 | 0.469 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.404 |
DOC_MAPK_gen_1 | 227 | 233 | PF00069 | 0.618 |
DOC_MAPK_gen_1 | 298 | 308 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 95 | 102 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 445 | 453 | PF00069 | 0.471 |
DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.396 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.671 |
DOC_USP7_UBL2_3 | 173 | 177 | PF12436 | 0.374 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.571 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.516 |
LIG_APCC_ABBA_1 | 449 | 454 | PF00400 | 0.430 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.459 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.473 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.463 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.402 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.708 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.529 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.438 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.664 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.490 |
LIG_LIR_Gen_1 | 375 | 383 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 394 | 403 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.428 |
LIG_PCNA_PIPBox_1 | 389 | 398 | PF02747 | 0.495 |
LIG_Pex14_2 | 379 | 383 | PF04695 | 0.455 |
LIG_SH2_GRB2like | 131 | 134 | PF00017 | 0.417 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 396 | 399 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.486 |
LIG_SH3_1 | 469 | 475 | PF00018 | 0.496 |
LIG_SH3_2 | 472 | 477 | PF14604 | 0.516 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.565 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.621 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 304 | 311 | PF11976 | 0.635 |
LIG_SUMO_SIM_anti_2 | 463 | 470 | PF11976 | 0.469 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.536 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.662 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.640 |
LIG_UBA3_1 | 417 | 426 | PF00899 | 0.444 |
LIG_WRC_WIRS_1 | 425 | 430 | PF05994 | 0.547 |
MOD_CDK_SPxK_1 | 471 | 477 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 312 | 319 | PF00069 | 0.512 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.473 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.692 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.668 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.666 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.643 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.650 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.504 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.612 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.635 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.453 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.581 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.745 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.445 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.462 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.536 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.491 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.540 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.367 |
MOD_GlcNHglycan | 195 | 199 | PF01048 | 0.412 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.719 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.713 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.520 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.619 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.535 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.655 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.586 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.645 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.595 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.697 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.487 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.515 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.388 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.593 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.255 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.255 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.639 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.483 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.570 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.511 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.415 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.434 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.580 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.547 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.658 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.635 |
MOD_Plk_2-3 | 235 | 241 | PF00069 | 0.723 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.712 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.639 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.605 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.653 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.738 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.455 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.520 |
MOD_SUMO_rev_2 | 13 | 23 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 313 | 322 | PF00179 | 0.705 |
MOD_SUMO_rev_2 | 478 | 486 | PF00179 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.547 |
TRG_ER_diLys_1 | 485 | 489 | PF00400 | 0.559 |
TRG_NLS_Bipartite_1 | 212 | 232 | PF00514 | 0.651 |
TRG_NLS_MonoCore_2 | 226 | 231 | PF00514 | 0.616 |
TRG_NLS_MonoExtC_3 | 297 | 302 | PF00514 | 0.508 |
TRG_NLS_MonoExtN_4 | 227 | 232 | PF00514 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.245 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF88 | Leptomonas seymouri | 60% | 99% |
A0A0S4J9Z5 | Bodo saltans | 40% | 100% |
A0A1X0NH58 | Trypanosomatidae | 40% | 100% |
A0A3Q8IHU4 | Leishmania donovani | 93% | 100% |
A0A3R7KY85 | Trypanosoma rangeli | 40% | 100% |
A4HG19 | Leishmania braziliensis | 82% | 100% |
A4I340 | Leishmania infantum | 94% | 100% |
C9ZJL2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AZE8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 98% |
Q28IV3 | Xenopus tropicalis | 25% | 74% |
Q68FQ7 | Rattus norvegicus | 26% | 74% |
Q6NU95 | Xenopus laevis | 25% | 74% |
Q9D706 | Mus musculus | 25% | 74% |
V5AR46 | Trypanosoma cruzi | 39% | 100% |