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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A0A3S7WRB9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.696 |
CLV_C14_Caspase3-7 | 387 | 391 | PF00656 | 0.479 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.773 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.672 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.722 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.695 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.593 |
DEG_SPOP_SBC_1 | 356 | 360 | PF00917 | 0.567 |
DEG_SPOP_SBC_1 | 585 | 589 | PF00917 | 0.542 |
DOC_MAPK_gen_1 | 494 | 500 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 196 | 203 | PF00069 | 0.585 |
DOC_PP1_RVXF_1 | 198 | 204 | PF00149 | 0.478 |
DOC_PP1_RVXF_1 | 446 | 453 | PF00149 | 0.643 |
DOC_PP1_RVXF_1 | 604 | 610 | PF00149 | 0.688 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.616 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 246 | 252 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 448 | 453 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 522 | 531 | PF00244 | 0.601 |
LIG_APCC_ABBA_1 | 199 | 204 | PF00400 | 0.485 |
LIG_eIF4E_1 | 373 | 379 | PF01652 | 0.668 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.566 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.592 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.682 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.522 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.534 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.797 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.771 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.390 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.607 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.701 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.674 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.649 |
LIG_GBD_Chelix_1 | 446 | 454 | PF00786 | 0.637 |
LIG_HCF-1_HBM_1 | 16 | 19 | PF13415 | 0.664 |
LIG_LIR_Gen_1 | 16 | 25 | PF02991 | 0.640 |
LIG_LIR_Gen_1 | 451 | 460 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.529 |
LIG_Pex14_2 | 333 | 337 | PF04695 | 0.499 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.514 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.654 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.791 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.585 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.651 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.720 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.646 |
LIG_SH3_3 | 604 | 610 | PF00018 | 0.688 |
LIG_SUMO_SIM_anti_2 | 250 | 255 | PF11976 | 0.721 |
LIG_SUMO_SIM_anti_2 | 575 | 580 | PF11976 | 0.658 |
LIG_TYR_ITIM | 374 | 379 | PF00017 | 0.742 |
LIG_WRC_WIRS_1 | 385 | 390 | PF05994 | 0.483 |
LIG_WRC_WIRS_1 | 449 | 454 | PF05994 | 0.593 |
LIG_WRC_WIRS_1 | 561 | 566 | PF05994 | 0.642 |
MOD_CDK_SPxxK_3 | 140 | 147 | PF00069 | 0.634 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.618 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.644 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.710 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.585 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.562 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.688 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.576 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.603 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.651 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.553 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.560 |
MOD_DYRK1A_RPxSP_1 | 569 | 573 | PF00069 | 0.678 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.720 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.649 |
MOD_GlcNHglycan | 234 | 238 | PF01048 | 0.712 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.661 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.633 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.497 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.679 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.584 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.712 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.630 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.513 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.699 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.635 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.615 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.690 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.704 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.729 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.679 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.675 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.606 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.583 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.659 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.463 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.545 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.473 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.530 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.635 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.621 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.612 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.570 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.728 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.659 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.545 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.550 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.512 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.669 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.661 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.729 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.597 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.670 |
MOD_Plk_1 | 537 | 543 | PF00069 | 0.633 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.721 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.597 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.779 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.462 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.431 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.531 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.751 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.647 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.738 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.691 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.737 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.478 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.609 |
MOD_SUMO_rev_2 | 56 | 60 | PF00179 | 0.729 |
TRG_DiLeu_BaLyEn_6 | 445 | 450 | PF01217 | 0.562 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.735 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSV0 | Leptomonas seymouri | 35% | 100% |
A4HUL1 | Leishmania infantum | 99% | 100% |
E9ANA8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QHB6 | Leishmania major | 89% | 100% |