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: A4I9R1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.451 |
CLV_C14_Caspase3-7 | 51 | 55 | PF00656 | 0.564 |
CLV_C14_Caspase3-7 | 99 | 103 | PF00656 | 0.593 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.524 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 26 | 28 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.469 |
CLV_Separin_Metazoa | 525 | 529 | PF03568 | 0.366 |
DEG_APCC_DBOX_1 | 582 | 590 | PF00400 | 0.394 |
DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.613 |
DOC_CKS1_1 | 203 | 208 | PF01111 | 0.605 |
DOC_CYCLIN_yCln2_LP_2 | 360 | 366 | PF00134 | 0.422 |
DOC_MAPK_MEF2A_6 | 353 | 360 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 84 | 91 | PF00069 | 0.429 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.595 |
DOC_USP7_UBL2_3 | 345 | 349 | PF12436 | 0.553 |
DOC_USP7_UBL2_3 | 399 | 403 | PF12436 | 0.607 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 141 | 149 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 192 | 200 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 275 | 279 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 427 | 435 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 448 | 458 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 479 | 487 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 546 | 555 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 583 | 593 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 597 | 601 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.449 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.509 |
LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.565 |
LIG_Clathr_ClatBox_1 | 335 | 339 | PF01394 | 0.447 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.504 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.632 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.569 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.425 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.540 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.698 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.418 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.767 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.464 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.563 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.646 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.429 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.517 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.378 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.457 |
LIG_GBD_Chelix_1 | 249 | 257 | PF00786 | 0.447 |
LIG_LIR_Apic_2 | 102 | 108 | PF02991 | 0.626 |
LIG_LIR_Gen_1 | 330 | 341 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 587 | 598 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 605 | 615 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 605 | 610 | PF02991 | 0.392 |
LIG_LYPXL_yS_3 | 355 | 358 | PF13949 | 0.397 |
LIG_PCNA_PIPBox_1 | 601 | 610 | PF02747 | 0.450 |
LIG_PCNA_yPIPBox_3 | 597 | 608 | PF02747 | 0.445 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 531 | 535 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 598 | 601 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.359 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.655 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.376 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.340 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.474 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.807 |
LIG_SUMO_SIM_anti_2 | 521 | 528 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 207 | 214 | PF11976 | 0.522 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.644 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.466 |
LIG_TRAF2_1 | 551 | 554 | PF00917 | 0.487 |
LIG_TRAF2_1 | 578 | 581 | PF00917 | 0.457 |
MOD_CDC14_SPxK_1 | 445 | 448 | PF00782 | 0.601 |
MOD_CDK_SPK_2 | 442 | 447 | PF00069 | 0.651 |
MOD_CDK_SPxK_1 | 442 | 448 | PF00069 | 0.608 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.669 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.572 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.666 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.588 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.608 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.577 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.647 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.446 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.518 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.615 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.584 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.592 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.767 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.647 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.587 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.590 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.478 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.584 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.449 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.326 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.459 |
MOD_DYRK1A_RPxSP_1 | 275 | 279 | PF00069 | 0.485 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.481 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.799 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.582 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.266 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.463 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.404 |
MOD_GlcNHglycan | 390 | 394 | PF01048 | 0.593 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.647 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.576 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.455 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.653 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.508 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.728 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.380 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.639 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.511 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.596 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.621 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.489 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.473 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.378 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.680 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.568 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.624 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.573 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.512 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.474 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.418 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.606 |
MOD_N-GLC_2 | 62 | 64 | PF02516 | 0.569 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.557 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.522 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.451 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.612 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.625 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.443 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.516 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.492 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.412 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.528 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.426 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.356 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.595 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.600 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.471 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.400 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.595 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.504 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.596 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.400 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.448 |
MOD_PKB_1 | 404 | 412 | PF00069 | 0.632 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.616 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.556 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.620 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.600 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.582 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.546 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.604 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.562 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.533 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.695 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.633 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.463 |
MOD_SUMO_rev_2 | 339 | 346 | PF00179 | 0.464 |
TRG_DiLeu_BaEn_4 | 222 | 228 | PF01217 | 0.645 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 531 | 534 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.524 |
TRG_NES_CRM1_1 | 370 | 383 | PF08389 | 0.443 |
TRG_NLS_MonoExtC_3 | 384 | 389 | PF00514 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 326 | 331 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P311 | Leptomonas seymouri | 41% | 98% |
A0A3S7X7P4 | Leishmania donovani | 100% | 100% |
A4HAL4 | Leishmania braziliensis | 68% | 100% |
E9B4S3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q3A4 | Leishmania major | 90% | 100% |