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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0035371 | microtubule plus-end | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990752 | microtubule end | 2 | 1 |
Related structures:
AlphaFold database: E9AS44
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097435 | supramolecular fiber organization | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008017 | microtubule binding | 5 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0051010 | microtubule plus-end binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 568 | 572 | PF00656 | 0.413 |
CLV_C14_Caspase3-7 | 633 | 637 | PF00656 | 0.545 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 643 | 647 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.460 |
DEG_SCF_FBW7_1 | 645 | 652 | PF00400 | 0.645 |
DEG_SCF_FBW7_2 | 24 | 31 | PF00400 | 0.365 |
DEG_SPOP_SBC_1 | 440 | 444 | PF00917 | 0.693 |
DOC_CKS1_1 | 25 | 30 | PF01111 | 0.373 |
DOC_CKS1_1 | 646 | 651 | PF01111 | 0.654 |
DOC_CYCLIN_RxL_1 | 467 | 477 | PF00134 | 0.599 |
DOC_CYCLIN_RxL_1 | 623 | 636 | PF00134 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 86 | 92 | PF00134 | 0.477 |
DOC_MAPK_gen_1 | 32 | 39 | PF00069 | 0.312 |
DOC_MAPK_gen_1 | 610 | 619 | PF00069 | 0.654 |
DOC_MAPK_MEF2A_6 | 613 | 621 | PF00069 | 0.604 |
DOC_MAPK_RevD_3 | 21 | 34 | PF00069 | 0.515 |
DOC_PP1_RVXF_1 | 626 | 633 | PF00149 | 0.528 |
DOC_PP1_SILK_1 | 34 | 39 | PF00149 | 0.388 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 646 | 649 | PF00568 | 0.650 |
DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.319 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.735 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.577 |
DOC_USP7_UBL2_3 | 191 | 195 | PF12436 | 0.383 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 645 | 650 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 424 | 431 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 510 | 514 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 581 | 586 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 596 | 605 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.611 |
LIG_Actin_WH2_2 | 130 | 147 | PF00022 | 0.531 |
LIG_DLG_GKlike_1 | 581 | 588 | PF00625 | 0.528 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.379 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.475 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.534 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.550 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.466 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.458 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.565 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.510 |
LIG_IRF3_LxIS_1 | 451 | 456 | PF10401 | 0.436 |
LIG_LIR_Apic_2 | 599 | 605 | PF02991 | 0.646 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.321 |
LIG_NRBOX | 360 | 366 | PF00104 | 0.468 |
LIG_NRBOX | 584 | 590 | PF00104 | 0.524 |
LIG_RPA_C_Fungi | 213 | 225 | PF08784 | 0.574 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.418 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.485 |
LIG_SH2_PTP2 | 603 | 606 | PF00017 | 0.514 |
LIG_SH2_SRC | 603 | 606 | PF00017 | 0.459 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 578 | 582 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 603 | 606 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.352 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.613 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.374 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.563 |
LIG_SUMO_SIM_anti_2 | 18 | 25 | PF11976 | 0.415 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.530 |
LIG_TRAF2_1 | 315 | 318 | PF00917 | 0.446 |
LIG_TRAF2_1 | 404 | 407 | PF00917 | 0.484 |
LIG_TYR_ITIM | 601 | 606 | PF00017 | 0.455 |
LIG_WRC_WIRS_1 | 17 | 22 | PF05994 | 0.422 |
MOD_CDK_SPK_2 | 547 | 552 | PF00069 | 0.457 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.614 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.483 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.370 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.503 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.754 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.516 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.483 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.427 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.555 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.509 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.207 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.505 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.712 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.637 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.589 |
MOD_GlcNHglycan | 266 | 270 | PF01048 | 0.432 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.576 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.571 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.593 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.717 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.588 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.450 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.605 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.461 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.566 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.722 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.478 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.644 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.671 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.634 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.540 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.624 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.523 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.386 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.613 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.507 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.524 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.521 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.495 |
MOD_PKA_1 | 218 | 224 | PF00069 | 0.440 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.386 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.562 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.658 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.584 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.581 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.524 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.661 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.482 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.521 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.423 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.587 |
MOD_Plk_2-3 | 449 | 455 | PF00069 | 0.587 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.448 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.389 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.539 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.466 |
MOD_ProDKin_1 | 645 | 651 | PF00069 | 0.684 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.533 |
MOD_SUMO_for_1 | 104 | 107 | PF00179 | 0.533 |
MOD_SUMO_for_1 | 157 | 160 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 184 | 193 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 366 | 374 | PF00179 | 0.466 |
TRG_DiLeu_BaEn_1 | 360 | 365 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_1 | 407 | 412 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_4 | 356 | 362 | PF01217 | 0.540 |
TRG_DiLeu_BaLyEn_6 | 625 | 630 | PF01217 | 0.612 |
TRG_DiLeu_LyEn_5 | 407 | 412 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 468 | 471 | PF00400 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 410 | 414 | PF00026 | 0.544 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSH8 | Leptomonas seymouri | 37% | 91% |
A0A3Q8IEJ2 | Leishmania donovani | 85% | 98% |
A4HA45 | Leishmania braziliensis | 71% | 97% |
A4HYB1 | Leishmania infantum | 85% | 98% |
Q4QDC2 | Leishmania major | 84% | 100% |