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: Q4Q6L3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 600 | 604 | PF00656 | 0.528 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.609 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 532 | 534 | PF00082 | 0.436 |
CLV_PCSK_PC7_1 | 221 | 227 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.650 |
DEG_APCC_DBOX_1 | 306 | 314 | PF00400 | 0.495 |
DOC_CYCLIN_yCln2_LP_2 | 343 | 349 | PF00134 | 0.561 |
DOC_MAPK_gen_1 | 511 | 518 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 532 | 539 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 532 | 539 | PF00069 | 0.501 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.515 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 627 | 631 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.632 |
DOC_USP7_UBL2_3 | 464 | 468 | PF12436 | 0.616 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 204 | 212 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 225 | 234 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 307 | 315 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 361 | 369 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 405 | 413 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 453 | 458 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 629 | 634 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 89 | 93 | PF00244 | 0.634 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.608 |
LIG_BRCT_BRCA1_2 | 90 | 96 | PF00533 | 0.669 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.639 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.501 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.651 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.544 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.733 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.585 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.495 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.512 |
LIG_FHA_2 | 581 | 587 | PF00498 | 0.621 |
LIG_Integrin_RGD_1 | 398 | 400 | PF01839 | 0.675 |
LIG_LIR_Gen_1 | 128 | 134 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.482 |
LIG_SH2_SRC | 546 | 549 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.529 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.640 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.591 |
LIG_SUMO_SIM_anti_2 | 128 | 134 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 428 | 434 | PF11976 | 0.646 |
LIG_SUMO_SIM_par_1 | 428 | 434 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 534 | 540 | PF11976 | 0.492 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.603 |
LIG_TRAF2_1 | 472 | 475 | PF00917 | 0.627 |
LIG_TRFH_1 | 320 | 324 | PF08558 | 0.610 |
LIG_WW_3 | 177 | 181 | PF00397 | 0.544 |
MOD_CDK_SPK_2 | 259 | 264 | PF00069 | 0.686 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.573 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.488 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.529 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.736 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.581 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.672 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.546 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.585 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.538 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.738 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.558 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.646 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.552 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.618 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.634 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.668 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.617 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.555 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.607 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.709 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.590 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.587 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.595 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.679 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.568 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.589 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.585 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.636 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.660 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.673 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.761 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.625 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.701 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.706 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.635 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.606 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.487 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.695 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.626 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.670 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.560 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.524 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.620 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.525 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.451 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.774 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.746 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.324 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.525 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.649 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.582 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.698 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.556 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.523 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.668 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.529 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.641 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.594 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.621 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.676 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.600 |
MOD_N-GLC_1 | 390 | 395 | PF02516 | 0.704 |
MOD_N-GLC_1 | 453 | 458 | PF02516 | 0.577 |
MOD_N-GLC_1 | 603 | 608 | PF02516 | 0.571 |
MOD_N-GLC_1 | 627 | 632 | PF02516 | 0.681 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.579 |
MOD_N-GLC_2 | 255 | 257 | PF02516 | 0.621 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.422 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.613 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.546 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.629 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.618 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.561 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.628 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.664 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.593 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.624 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.394 |
MOD_PIKK_1 | 324 | 330 | PF00454 | 0.576 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.700 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.671 |
MOD_PKA_1 | 204 | 210 | PF00069 | 0.614 |
MOD_PKA_1 | 225 | 231 | PF00069 | 0.588 |
MOD_PKA_1 | 405 | 411 | PF00069 | 0.657 |
MOD_PKA_1 | 569 | 575 | PF00069 | 0.606 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.622 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.614 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.400 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.619 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.688 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.721 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.642 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.603 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.620 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.433 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.616 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.581 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.565 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.601 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.552 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.580 |
MOD_Plk_2-3 | 332 | 338 | PF00069 | 0.587 |
MOD_Plk_2-3 | 339 | 345 | PF00069 | 0.520 |
MOD_Plk_2-3 | 475 | 481 | PF00069 | 0.682 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.456 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.463 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.412 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.712 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.697 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.706 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.709 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.569 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.650 |
MOD_SUMO_rev_2 | 140 | 150 | PF00179 | 0.637 |
MOD_SUMO_rev_2 | 458 | 466 | PF00179 | 0.593 |
MOD_SUMO_rev_2 | 70 | 77 | PF00179 | 0.607 |
TRG_DiLeu_BaEn_2 | 279 | 285 | PF01217 | 0.423 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.652 |
TRG_Pf-PMV_PEXEL_1 | 504 | 508 | PF00026 | 0.650 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA33 | Leptomonas seymouri | 44% | 100% |
A0A3S7X488 | Leishmania donovani | 92% | 100% |
A4HJ28 | Leishmania braziliensis | 61% | 99% |
A4I6K7 | Leishmania infantum | 92% | 100% |
E9B1K0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |