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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005819 | spindle | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AKS2
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0007018 | microtubule-based movement | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003774 | cytoskeletal motor activity | 1 | 2 |
GO:0003777 | microtubule motor activity | 2 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0008017 | microtubule binding | 5 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:0140657 | ATP-dependent activity | 1 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 190 | 194 | PF00656 | 0.751 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.622 |
CLV_PCSK_FUR_1 | 422 | 426 | PF00082 | 0.571 |
CLV_PCSK_FUR_1 | 635 | 639 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 609 | 611 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.447 |
DEG_APCC_KENBOX_2 | 196 | 200 | PF00400 | 0.768 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.601 |
DEG_SPOP_SBC_1 | 13 | 17 | PF00917 | 0.815 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.661 |
DEG_SPOP_SBC_1 | 86 | 90 | PF00917 | 0.604 |
DOC_CYCLIN_yCln2_LP_2 | 356 | 362 | PF00134 | 0.411 |
DOC_MAPK_DCC_7 | 352 | 362 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 304 | 312 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 608 | 619 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 540 | 548 | PF00069 | 0.456 |
DOC_PP4_FxxP_1 | 255 | 258 | PF00568 | 0.489 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.757 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.578 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 113 | 121 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 150 | 155 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 304 | 308 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 388 | 396 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 540 | 548 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 6 | 11 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 60 | 70 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 626 | 633 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 643 | 651 | PF00244 | 0.512 |
LIG_14-3-3_CterR_2 | 686 | 691 | PF00244 | 0.674 |
LIG_Actin_WH2_2 | 562 | 577 | PF00022 | 0.558 |
LIG_BIR_III_4 | 193 | 197 | PF00653 | 0.752 |
LIG_BRCT_BRCA1_1 | 102 | 106 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.395 |
LIG_BRCT_BRCA1_1 | 509 | 513 | PF00533 | 0.566 |
LIG_DLG_GKlike_1 | 6 | 14 | PF00625 | 0.554 |
LIG_EH1_1 | 396 | 404 | PF00400 | 0.427 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.791 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.612 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.377 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.356 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.460 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.540 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.656 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.781 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.355 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.383 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.595 |
LIG_LIR_Apic_2 | 153 | 158 | PF02991 | 0.444 |
LIG_LIR_Apic_2 | 254 | 258 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 137 | 146 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 309 | 318 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 510 | 519 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.508 |
LIG_NRBOX | 352 | 358 | PF00104 | 0.356 |
LIG_Pex14_1 | 102 | 106 | PF04695 | 0.475 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.469 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 296 | 300 | PF00017 | 0.464 |
LIG_SH2_PTP2 | 138 | 141 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 364 | 367 | PF00017 | 0.382 |
LIG_SH2_SRC | 121 | 124 | PF00017 | 0.476 |
LIG_SH2_SRC | 296 | 299 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.682 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.528 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.419 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.305 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.469 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.433 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.333 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.377 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.734 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.615 |
LIG_SUMO_SIM_par_1 | 366 | 372 | PF11976 | 0.466 |
LIG_TYR_ITIM | 362 | 367 | PF00017 | 0.406 |
LIG_UBA3_1 | 173 | 182 | PF00899 | 0.572 |
LIG_UBA3_1 | 603 | 611 | PF00899 | 0.589 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.476 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.311 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.739 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.739 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.387 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.360 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.389 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.528 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.557 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.521 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.375 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.678 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.696 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.801 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.796 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.482 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.371 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.563 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.496 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.456 |
MOD_Cter_Amidation | 302 | 305 | PF01082 | 0.469 |
MOD_Cter_Amidation | 606 | 609 | PF01082 | 0.577 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.442 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.382 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.675 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.780 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.801 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.601 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.404 |
MOD_GlcNHglycan | 547 | 551 | PF01048 | 0.542 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.573 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.578 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.642 |
MOD_GlcNHglycan | 681 | 684 | PF01048 | 0.704 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.644 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.783 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.460 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.664 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.450 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.624 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.731 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.535 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.511 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.428 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.548 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.505 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.605 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.580 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.602 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.660 |
MOD_LATS_1 | 51 | 57 | PF00433 | 0.489 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.445 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.527 |
MOD_N-GLC_1 | 450 | 455 | PF02516 | 0.589 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.461 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.297 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.513 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.434 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.661 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.558 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.592 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.522 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.650 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.657 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.449 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.748 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.504 |
MOD_PIKK_1 | 522 | 528 | PF00454 | 0.451 |
MOD_PIKK_1 | 535 | 541 | PF00454 | 0.508 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.601 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.714 |
MOD_PIKK_1 | 674 | 680 | PF00454 | 0.666 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.750 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.760 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.412 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.538 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.573 |
MOD_PKA_2 | 625 | 631 | PF00069 | 0.605 |
MOD_PKA_2 | 636 | 642 | PF00069 | 0.444 |
MOD_PKA_2 | 654 | 660 | PF00069 | 0.656 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.442 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.377 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.486 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.456 |
MOD_Plk_1 | 587 | 593 | PF00069 | 0.621 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.449 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.391 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.498 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.405 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.359 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.732 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 276 | 285 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 345 | 354 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 547 | 555 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 566 | 571 | PF00179 | 0.271 |
MOD_SUMO_rev_2 | 670 | 676 | PF00179 | 0.497 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.365 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.471 |
TRG_ER_diArg_1 | 265 | 268 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 421 | 424 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 516 | 518 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 610 | 613 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 637 | 640 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 70 | 73 | PF00400 | 0.577 |
TRG_NLS_MonoCore_2 | 607 | 612 | PF00514 | 0.600 |
TRG_NLS_MonoExtC_3 | 607 | 612 | PF00514 | 0.557 |
TRG_NLS_MonoExtN_4 | 608 | 613 | PF00514 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 409 | 413 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 517 | 521 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC06 | Leptomonas seymouri | 71% | 99% |
A0A0S4KIG4 | Bodo saltans | 29% | 94% |
A0A1X0NKL3 | Trypanosomatidae | 54% | 100% |
A0A3R7LWH4 | Trypanosoma rangeli | 52% | 100% |
A0A3S5H5Q4 | Leishmania donovani | 96% | 100% |
A4H4K9 | Leishmania braziliensis | 88% | 99% |
A4HST5 | Leishmania infantum | 97% | 100% |
C9ZTE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
Q4QJ35 | Leishmania major | 95% | 100% |
V5DPG4 | Trypanosoma cruzi | 52% | 100% |