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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B5A6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0008104 | protein localization | 4 | 7 |
GO:0009306 | protein secretion | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0015031 | protein transport | 4 | 7 |
GO:0030254 | protein secretion by the type III secretion system | 4 | 7 |
GO:0032940 | secretion by cell | 3 | 7 |
GO:0033036 | macromolecule localization | 2 | 7 |
GO:0035592 | establishment of protein localization to extracellular region | 4 | 7 |
GO:0045184 | establishment of protein localization | 3 | 7 |
GO:0046903 | secretion | 4 | 7 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
GO:0051641 | cellular localization | 2 | 7 |
GO:0055085 | transmembrane transport | 2 | 7 |
GO:0070727 | cellular macromolecule localization | 3 | 7 |
GO:0071692 | protein localization to extracellular region | 5 | 7 |
GO:0071702 | organic substance transport | 4 | 7 |
GO:0071705 | nitrogen compound transport | 4 | 7 |
GO:0071806 | protein transmembrane transport | 3 | 7 |
GO:0140352 | export from cell | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 18 | 22 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.387 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.444 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.588 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.411 |
CLV_PCSK_PC7_1 | 132 | 138 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 327 | 333 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.440 |
DEG_APCC_DBOX_1 | 263 | 271 | PF00400 | 0.465 |
DEG_APCC_DBOX_1 | 372 | 380 | PF00400 | 0.452 |
DEG_APCC_DBOX_1 | 496 | 504 | PF00400 | 0.475 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.658 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.507 |
DOC_CYCLIN_RxL_1 | 315 | 329 | PF00134 | 0.432 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 288 | 296 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 465 | 473 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 475 | 484 | PF00069 | 0.520 |
DOC_PP2B_LxvP_1 | 119 | 122 | PF13499 | 0.494 |
DOC_PP2B_LxvP_1 | 149 | 152 | PF13499 | 0.536 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.600 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.459 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 148 | 152 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 373 | 377 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 537 | 544 | PF00244 | 0.434 |
LIG_Actin_WH2_2 | 523 | 539 | PF00022 | 0.529 |
LIG_BRCT_BRCA1_1 | 402 | 406 | PF00533 | 0.542 |
LIG_Clathr_ClatBox_1 | 470 | 474 | PF01394 | 0.475 |
LIG_CtBP_PxDLS_1 | 210 | 214 | PF00389 | 0.612 |
LIG_eIF4E_1 | 481 | 487 | PF01652 | 0.495 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.464 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.383 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.553 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.510 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.462 |
LIG_LIR_Gen_1 | 385 | 394 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 478 | 487 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 59 | 65 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 478 | 484 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.491 |
LIG_SH2_CRK | 207 | 211 | PF00017 | 0.613 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 191 | 195 | PF00017 | 0.563 |
LIG_SH2_PTP2 | 483 | 486 | PF00017 | 0.529 |
LIG_SH2_SRC | 481 | 484 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.596 |
LIG_SH2_STAT3 | 439 | 442 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.526 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.556 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.666 |
LIG_SUMO_SIM_anti_2 | 322 | 329 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 524 | 531 | PF11976 | 0.466 |
LIG_SUMO_SIM_anti_2 | 561 | 566 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 208 | 214 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 448 | 453 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 469 | 474 | PF11976 | 0.475 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.530 |
LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.472 |
LIG_WW_3 | 121 | 125 | PF00397 | 0.559 |
MOD_CDC14_SPxK_1 | 134 | 137 | PF00782 | 0.561 |
MOD_CDK_SPK_2 | 131 | 136 | PF00069 | 0.701 |
MOD_CDK_SPK_2 | 143 | 148 | PF00069 | 0.550 |
MOD_CDK_SPK_2 | 163 | 168 | PF00069 | 0.513 |
MOD_CDK_SPxK_1 | 131 | 137 | PF00069 | 0.568 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.595 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.483 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.651 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.500 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.434 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.566 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.661 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.464 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.513 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.468 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.647 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.658 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.650 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.457 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.481 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.200 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.291 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.474 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.485 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.509 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.617 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.609 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.721 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.500 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.400 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.275 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.585 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.644 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.567 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.578 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.600 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.487 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.495 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.555 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.561 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.496 |
MOD_NEK2_2 | 297 | 302 | PF00069 | 0.388 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.423 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.644 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.518 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.514 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.616 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.529 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.492 |
MOD_Plk_2-3 | 382 | 388 | PF00069 | 0.442 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.493 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.597 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.275 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.520 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.590 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.701 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.756 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.582 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.681 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.605 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.709 |
MOD_SUMO_for_1 | 314 | 317 | PF00179 | 0.431 |
MOD_SUMO_for_1 | 358 | 361 | PF00179 | 0.525 |
MOD_SUMO_rev_2 | 248 | 254 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 280 | 290 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 335 | 344 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_4 | 285 | 291 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.578 |
TRG_ER_diArg_1 | 135 | 137 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.453 |
TRG_NES_CRM1_1 | 248 | 259 | PF08389 | 0.503 |
TRG_NES_CRM1_1 | 55 | 67 | PF08389 | 0.469 |
TRG_NLS_MonoExtC_3 | 38 | 43 | PF00514 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 356 | 361 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IIE0 | Leishmania donovani | 86% | 100% |
A4HB36 | Leishmania braziliensis | 72% | 100% |
A4IAN3 | Leishmania infantum | 86% | 100% |
Q4Q2M7 | Leishmania major | 85% | 100% |
V5BKV7 | Trypanosoma cruzi | 34% | 100% |