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 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0035371 | microtubule plus-end | 3 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1990752 | microtubule end | 2 | 2 |
Related structures:
AlphaFold database: Q4QDC2
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008017 | microtubule binding | 5 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0051010 | microtubule plus-end binding | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 153 | 157 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 376 | 380 | PF00656 | 0.409 |
CLV_C14_Caspase3-7 | 635 | 639 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.304 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.304 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.325 |
DEG_SCF_FBW7_1 | 647 | 654 | PF00400 | 0.588 |
DEG_SCF_FBW7_2 | 95 | 100 | PF00400 | 0.461 |
DEG_SIAH_1 | 560 | 568 | PF03145 | 0.506 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.590 |
DOC_CKS1_1 | 648 | 653 | PF01111 | 0.632 |
DOC_CYCLIN_RxL_1 | 469 | 480 | PF00134 | 0.577 |
DOC_CYCLIN_RxL_1 | 625 | 638 | PF00134 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 86 | 92 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 279 | 288 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 32 | 39 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 583 | 592 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 612 | 621 | PF00069 | 0.639 |
DOC_MAPK_MEF2A_6 | 452 | 459 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 615 | 623 | PF00069 | 0.592 |
DOC_MAPK_RevD_3 | 21 | 34 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 174 | 180 | PF00149 | 0.466 |
DOC_PP1_RVXF_1 | 628 | 635 | PF00149 | 0.519 |
DOC_PP1_SILK_1 | 34 | 39 | PF00149 | 0.369 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.419 |
DOC_PP4_FxxP_1 | 648 | 651 | PF00568 | 0.664 |
DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.304 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.631 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.574 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.472 |
LIG_14-3-3_CanoR_1 | 181 | 190 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 512 | 516 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 583 | 588 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 598 | 607 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.561 |
LIG_Actin_WH2_2 | 130 | 147 | PF00022 | 0.543 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.643 |
LIG_DLG_GKlike_1 | 583 | 590 | PF00625 | 0.513 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.543 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.508 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.463 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.405 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.590 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.439 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.539 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.513 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.408 |
LIG_LIR_Apic_2 | 601 | 607 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.318 |
LIG_NRBOX | 362 | 368 | PF00104 | 0.467 |
LIG_NRBOX | 586 | 592 | PF00104 | 0.509 |
LIG_RPA_C_Fungi | 213 | 225 | PF08784 | 0.539 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.450 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 580 | 584 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.348 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.553 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.362 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.469 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.449 |
LIG_SUMO_SIM_anti_2 | 18 | 25 | PF11976 | 0.394 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.508 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.513 |
LIG_TRAF2_1 | 406 | 409 | PF00917 | 0.484 |
LIG_WRC_WIRS_1 | 17 | 22 | PF05994 | 0.401 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.541 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.467 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.655 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.426 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.407 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.565 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.508 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.440 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.582 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.562 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.366 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.499 |
MOD_GlcNHglycan | 266 | 270 | PF01048 | 0.425 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.558 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.575 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.581 |
MOD_GlcNHglycan | 642 | 645 | PF01048 | 0.519 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.686 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.558 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.530 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.555 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.676 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.632 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.457 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.466 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.622 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.588 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.524 |
MOD_N-GLC_1 | 572 | 577 | PF02516 | 0.427 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.532 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.544 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.493 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.454 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.503 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.246 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.507 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.399 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.532 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.620 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.568 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.575 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.474 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.606 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.495 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.579 |
MOD_Plk_2-3 | 451 | 457 | PF00069 | 0.564 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.407 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.666 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.474 |
MOD_SUMO_for_1 | 104 | 107 | PF00179 | 0.508 |
MOD_SUMO_for_1 | 157 | 160 | PF00179 | 0.583 |
MOD_SUMO_for_1 | 343 | 346 | PF00179 | 0.509 |
MOD_SUMO_rev_2 | 187 | 193 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 368 | 376 | PF00179 | 0.469 |
TRG_DiLeu_BaEn_1 | 362 | 367 | PF01217 | 0.465 |
TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_4 | 358 | 364 | PF01217 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 627 | 632 | PF01217 | 0.593 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 470 | 473 | PF00400 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 415 | 419 | PF00026 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 585 | 589 | PF00026 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSH8 | Leptomonas seymouri | 35% | 91% |
A0A3Q8IEJ2 | Leishmania donovani | 88% | 98% |
A4HA45 | Leishmania braziliensis | 67% | 100% |
A4HYB1 | Leishmania infantum | 89% | 98% |
E9AS44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |