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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3Q8IBR0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.582 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.496 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.419 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.430 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.467 |
DEG_APCC_DBOX_1 | 307 | 315 | PF00400 | 0.362 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.466 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.592 |
DOC_CDC14_PxL_1 | 613 | 621 | PF14671 | 0.378 |
DOC_CKS1_1 | 499 | 504 | PF01111 | 0.460 |
DOC_CYCLIN_RxL_1 | 573 | 585 | PF00134 | 0.450 |
DOC_CYCLIN_RxL_1 | 628 | 636 | PF00134 | 0.406 |
DOC_CYCLIN_yCln2_LP_2 | 489 | 495 | PF00134 | 0.363 |
DOC_MAPK_DCC_7 | 640 | 649 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 308 | 315 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 40 | 47 | PF00069 | 0.460 |
DOC_MAPK_NFAT4_5 | 308 | 316 | PF00069 | 0.394 |
DOC_PP2B_LxvP_1 | 302 | 305 | PF13499 | 0.406 |
DOC_PP2B_LxvP_1 | 9 | 12 | PF13499 | 0.594 |
DOC_PP4_FxxP_1 | 286 | 289 | PF00568 | 0.420 |
DOC_PP4_FxxP_1 | 499 | 502 | PF00568 | 0.503 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.509 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 181 | 190 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 308 | 314 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 33 | 43 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 391 | 396 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 51 | 56 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 567 | 572 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 578 | 583 | PF00244 | 0.270 |
LIG_Actin_WH2_2 | 309 | 327 | PF00022 | 0.368 |
LIG_Actin_WH2_2 | 482 | 498 | PF00022 | 0.422 |
LIG_APCC_ABBA_1 | 43 | 48 | PF00400 | 0.448 |
LIG_APCC_ABBA_1 | 580 | 585 | PF00400 | 0.393 |
LIG_APCC_ABBA_1 | 610 | 615 | PF00400 | 0.455 |
LIG_BIR_III_2 | 538 | 542 | PF00653 | 0.354 |
LIG_eIF4E_1 | 359 | 365 | PF01652 | 0.504 |
LIG_eIF4E_1 | 613 | 619 | PF01652 | 0.412 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.606 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.433 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.423 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.474 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.542 |
LIG_GBD_Chelix_1 | 95 | 103 | PF00786 | 0.527 |
LIG_LIR_Gen_1 | 142 | 148 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 531 | 542 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 590 | 598 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 590 | 594 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.345 |
LIG_NRBOX | 451 | 457 | PF00104 | 0.454 |
LIG_Pex14_1 | 512 | 516 | PF04695 | 0.433 |
LIG_SH2_CRK | 359 | 363 | PF00017 | 0.468 |
LIG_SH2_GRB2like | 326 | 329 | PF00017 | 0.410 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.473 |
LIG_SH2_SRC | 613 | 616 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 326 | 330 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 419 | 423 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 516 | 520 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.441 |
LIG_SH3_1 | 406 | 412 | PF00018 | 0.481 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.365 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.481 |
LIG_SH3_3 | 640 | 646 | PF00018 | 0.322 |
LIG_Sin3_3 | 300 | 307 | PF02671 | 0.475 |
LIG_Sin3_3 | 434 | 441 | PF02671 | 0.386 |
LIG_SUMO_SIM_anti_2 | 451 | 456 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 214 | 221 | PF11976 | 0.353 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.634 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.419 |
LIG_TRFH_1 | 171 | 175 | PF08558 | 0.456 |
LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.496 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.567 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.582 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.456 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.410 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.405 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.352 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.482 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.503 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.406 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.473 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.440 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.284 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.495 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.270 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.591 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.505 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.446 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.544 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.644 |
MOD_Cter_Amidation | 15 | 18 | PF01082 | 0.735 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.564 |
MOD_GlcNHglycan | 13 | 17 | PF01048 | 0.658 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.516 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.413 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.386 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.277 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.442 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.377 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.479 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.631 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.421 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.449 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.489 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.420 |
MOD_GlcNHglycan | 595 | 599 | PF01048 | 0.474 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.656 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.529 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.586 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.600 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.480 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.444 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.418 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.297 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.382 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.588 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.543 |
MOD_LATS_1 | 100 | 106 | PF00433 | 0.435 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.370 |
MOD_N-GLC_2 | 577 | 579 | PF02516 | 0.317 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.417 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.433 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.438 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.399 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.537 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.497 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.280 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.453 |
MOD_NEK2_2 | 232 | 237 | PF00069 | 0.387 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.552 |
MOD_PK_1 | 51 | 57 | PF00069 | 0.494 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.435 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.786 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.442 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.371 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.567 |
MOD_Plk_1 | 624 | 630 | PF00069 | 0.470 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.447 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.388 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.499 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.534 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.517 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.390 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.451 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.480 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.500 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.368 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.565 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.477 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.497 |
TRG_DiLeu_BaEn_1 | 615 | 620 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 286 | 291 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 614 | 619 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 643 | 648 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 99 | 104 | PF01217 | 0.500 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.332 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 456 | 459 | PF00400 | 0.433 |
TRG_NES_CRM1_1 | 35 | 48 | PF08389 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 194 | 199 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 237 | 242 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 631 | 636 | PF00026 | 0.397 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKS3 | Leptomonas seymouri | 53% | 78% |
A0A1X0NXC2 | Trypanosomatidae | 26% | 83% |
A0A3R7RJS0 | Trypanosoma rangeli | 28% | 82% |
A4HD37 | Leishmania braziliensis | 86% | 100% |
C9ZNR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 80% |
E9AH15 | Leishmania infantum | 100% | 100% |
E9AWI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QAY5 | Leishmania major | 94% | 100% |
V5BFS5 | Trypanosoma cruzi | 26% | 82% |