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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 1 |
GO:0005876 | spindle microtubule | 7 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IH06
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
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:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 6 |
GO:0016874 | ligase activity | 2 | 9 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 6 |
GO:0016881 | acid-amino acid ligase activity | 4 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.725 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.761 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.725 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.701 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.339 |
CLV_PCSK_PC1ET2_1 | 628 | 630 | PF00082 | 0.507 |
CLV_PCSK_PC7_1 | 210 | 216 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.759 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.498 |
DEG_APCC_DBOX_1 | 349 | 357 | PF00400 | 0.564 |
DEG_APCC_DBOX_1 | 454 | 462 | PF00400 | 0.499 |
DEG_APCC_DBOX_1 | 504 | 512 | PF00400 | 0.493 |
DEG_SCF_FBW7_1 | 296 | 301 | PF00400 | 0.517 |
DEG_SPOP_SBC_1 | 105 | 109 | PF00917 | 0.720 |
DEG_SPOP_SBC_1 | 81 | 85 | PF00917 | 0.804 |
DOC_CYCLIN_RxL_1 | 153 | 161 | PF00134 | 0.486 |
DOC_CYCLIN_RxL_1 | 350 | 361 | PF00134 | 0.542 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 580 | 589 | PF00134 | 0.413 |
DOC_MAPK_gen_1 | 626 | 636 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 234 | 243 | PF00069 | 0.631 |
DOC_MAPK_MEF2A_6 | 608 | 615 | PF00069 | 0.456 |
DOC_MAPK_NFAT4_5 | 608 | 616 | PF00069 | 0.457 |
DOC_PP1_RVXF_1 | 252 | 259 | PF00149 | 0.485 |
DOC_PP1_RVXF_1 | 352 | 359 | PF00149 | 0.539 |
DOC_PP1_SILK_1 | 350 | 355 | PF00149 | 0.564 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.593 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.568 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 118 | 123 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 12 | 21 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 163 | 169 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 234 | 239 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 263 | 268 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 524 | 529 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 72 | 76 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 96 | 101 | PF00244 | 0.678 |
LIG_Actin_WH2_2 | 252 | 270 | PF00022 | 0.393 |
LIG_APCC_ABBA_1 | 400 | 405 | PF00400 | 0.499 |
LIG_APCC_ABBA_1 | 526 | 531 | PF00400 | 0.433 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.687 |
LIG_CaM_NSCaTE_8 | 588 | 595 | PF13499 | 0.418 |
LIG_eIF4E_1 | 373 | 379 | PF01652 | 0.474 |
LIG_eIF4E_1 | 401 | 407 | PF01652 | 0.474 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.707 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.496 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.437 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.539 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.523 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.441 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.517 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.457 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.377 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.484 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.633 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.493 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.620 |
LIG_Integrin_RGD_1 | 346 | 348 | PF01839 | 0.317 |
LIG_Integrin_RGD_1 | 491 | 493 | PF01839 | 0.317 |
LIG_LIR_Apic_2 | 233 | 239 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 149 | 159 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 161 | 169 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 569 | 580 | PF02991 | 0.353 |
LIG_LIR_LC3C_4 | 175 | 180 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 348 | 352 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 476 | 481 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.365 |
LIG_Pex14_2 | 575 | 579 | PF04695 | 0.374 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.603 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.652 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.564 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.517 |
LIG_SH2_CRK | 577 | 581 | PF00017 | 0.349 |
LIG_SH2_GRB2like | 500 | 503 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 236 | 240 | PF00017 | 0.603 |
LIG_SH2_NCK_1 | 25 | 29 | PF00017 | 0.622 |
LIG_SH2_PTP2 | 633 | 636 | PF00017 | 0.418 |
LIG_SH2_SRC | 447 | 450 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 577 | 581 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.226 |
LIG_SH3_2 | 486 | 491 | PF14604 | 0.517 |
LIG_SH3_2 | 596 | 601 | PF14604 | 0.515 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.564 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.525 |
LIG_SH3_3 | 491 | 497 | PF00018 | 0.525 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.547 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.491 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.366 |
LIG_SUMO_SIM_par_1 | 524 | 531 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 533 | 538 | PF11976 | 0.514 |
LIG_TRFH_1 | 294 | 298 | PF08558 | 0.539 |
MOD_CDK_SPK_2 | 480 | 485 | PF00069 | 0.525 |
MOD_CDK_SPxxK_3 | 235 | 242 | PF00069 | 0.673 |
MOD_CDK_SPxxK_3 | 421 | 428 | PF00069 | 0.564 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.575 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.718 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.474 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.541 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.538 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.436 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.608 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.525 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.601 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.645 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.725 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.773 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.497 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.354 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.597 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.477 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.657 |
MOD_Cter_Amidation | 38 | 41 | PF01082 | 0.643 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.706 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.654 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.592 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.510 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.678 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.302 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.291 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.789 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.616 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.582 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.658 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.495 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.651 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.694 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.391 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.517 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.489 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.559 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.392 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.599 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.632 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.589 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.622 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.658 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.669 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.588 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.328 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.259 |
MOD_N-GLC_2 | 434 | 436 | PF02516 | 0.274 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.692 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.657 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.446 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.590 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.474 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.474 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.539 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.477 |
MOD_NEK2_2 | 106 | 111 | PF00069 | 0.622 |
MOD_NEK2_2 | 464 | 469 | PF00069 | 0.564 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.524 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.499 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.622 |
MOD_PK_1 | 170 | 176 | PF00069 | 0.599 |
MOD_PK_1 | 409 | 415 | PF00069 | 0.474 |
MOD_PK_1 | 524 | 530 | PF00069 | 0.493 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.683 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.552 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.500 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.629 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.528 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.474 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.474 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.555 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.525 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.656 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.683 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.714 |
MOD_PKB_1 | 116 | 124 | PF00069 | 0.602 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.396 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.495 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.504 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.493 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.506 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.678 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.517 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.673 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.562 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.549 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.626 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.641 |
MOD_SUMO_for_1 | 473 | 476 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 85 | 94 | PF00179 | 0.640 |
TRG_DiLeu_BaEn_1 | 305 | 310 | PF01217 | 0.499 |
TRG_DiLeu_BaEn_4 | 448 | 454 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 374 | 379 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.683 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.416 |
TRG_NES_CRM1_1 | 307 | 322 | PF08389 | 0.457 |
TRG_NLS_MonoExtN_4 | 123 | 129 | PF00514 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8M9 | Leptomonas seymouri | 63% | 100% |
A0A1X0NRN8 | Trypanosomatidae | 41% | 100% |
A0A422NZN7 | Trypanosoma rangeli | 39% | 100% |
A4HKT5 | Leishmania braziliensis | 86% | 100% |
A4I8B4 | Leishmania infantum | 100% | 100% |
E9B373 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q4Y1 | Leishmania major | 96% | 100% |