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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 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 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IDV4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 18 |
GO:0006259 | DNA metabolic process | 4 | 18 |
GO:0006281 | DNA repair | 5 | 18 |
GO:0006310 | DNA recombination | 5 | 18 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 18 |
GO:0006807 | nitrogen compound metabolic process | 2 | 18 |
GO:0006950 | response to stress | 2 | 18 |
GO:0006974 | DNA damage response | 4 | 18 |
GO:0008152 | metabolic process | 1 | 18 |
GO:0009987 | cellular process | 1 | 18 |
GO:0033554 | cellular response to stress | 3 | 18 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 18 |
GO:0043170 | macromolecule metabolic process | 3 | 18 |
GO:0044237 | cellular metabolic process | 2 | 18 |
GO:0044238 | primary metabolic process | 2 | 18 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 18 |
GO:0046483 | heterocycle metabolic process | 3 | 18 |
GO:0050896 | response to stimulus | 1 | 18 |
GO:0051716 | cellular response to stimulus | 2 | 18 |
GO:0071704 | organic substance metabolic process | 2 | 18 |
GO:0090304 | nucleic acid metabolic process | 4 | 18 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 18 |
GO:0003824 | catalytic activity | 1 | 18 |
GO:0003909 | DNA ligase activity | 4 | 18 |
GO:0003910 | DNA ligase (ATP) activity | 5 | 18 |
GO:0005488 | binding | 1 | 18 |
GO:0005524 | ATP binding | 5 | 18 |
GO:0016874 | ligase activity | 2 | 18 |
GO:0016886 | ligase activity, forming phosphoric ester bonds | 3 | 18 |
GO:0017076 | purine nucleotide binding | 4 | 18 |
GO:0030554 | adenyl nucleotide binding | 5 | 18 |
GO:0032553 | ribonucleotide binding | 3 | 18 |
GO:0032555 | purine ribonucleotide binding | 4 | 18 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 18 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 18 |
GO:0036094 | small molecule binding | 2 | 18 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043168 | anion binding | 3 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:0097367 | carbohydrate derivative binding | 2 | 18 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 18 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 18 |
GO:1901265 | nucleoside phosphate binding | 3 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 196 | 200 | PF00656 | 0.443 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.468 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 584 | 586 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.773 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.344 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.758 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.716 |
CLV_PCSK_PC1ET2_1 | 499 | 501 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 583 | 585 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.342 |
DEG_APCC_DBOX_1 | 208 | 216 | PF00400 | 0.372 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.700 |
DEG_SCF_FBW7_1 | 574 | 579 | PF00400 | 0.417 |
DOC_ANK_TNKS_1 | 620 | 627 | PF00023 | 0.544 |
DOC_CDC14_PxL_1 | 14 | 22 | PF14671 | 0.472 |
DOC_CKS1_1 | 377 | 382 | PF01111 | 0.540 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 209 | 215 | PF00134 | 0.384 |
DOC_MAPK_gen_1 | 108 | 114 | PF00069 | 0.342 |
DOC_MAPK_RevD_3 | 461 | 474 | PF00069 | 0.398 |
DOC_PP1_RVXF_1 | 250 | 257 | PF00149 | 0.430 |
DOC_PP1_RVXF_1 | 90 | 97 | PF00149 | 0.306 |
DOC_SPAK_OSR1_1 | 571 | 575 | PF12202 | 0.417 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.715 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.528 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.377 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.463 |
DOC_USP7_UBL2_3 | 340 | 344 | PF12436 | 0.652 |
DOC_USP7_UBL2_3 | 591 | 595 | PF12436 | 0.478 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 562 | 567 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.319 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 421 | 431 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 527 | 532 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 571 | 575 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 585 | 591 | PF00244 | 0.222 |
LIG_Actin_WH2_2 | 427 | 445 | PF00022 | 0.489 |
LIG_BRCT_BRCA1_1 | 398 | 402 | PF00533 | 0.544 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.426 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.492 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.385 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.680 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.564 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.483 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.307 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.690 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.345 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.322 |
LIG_LIR_Apic_2 | 374 | 380 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 199 | 207 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 539 | 548 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 560 | 566 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 600 | 611 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 413 | 419 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 560 | 564 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 589 | 593 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 600 | 606 | PF02991 | 0.329 |
LIG_LYPXL_yS_3 | 17 | 20 | PF13949 | 0.471 |
LIG_NRBOX | 418 | 424 | PF00104 | 0.463 |
LIG_PDZ_Class_3 | 625 | 630 | PF00595 | 0.542 |
LIG_PDZ_Wminus1_1 | 628 | 630 | PF00595 | 0.505 |
LIG_Pex14_1 | 590 | 594 | PF04695 | 0.417 |
LIG_Pex14_2 | 557 | 561 | PF04695 | 0.288 |
LIG_REV1ctd_RIR_1 | 254 | 263 | PF16727 | 0.379 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.470 |
LIG_SH2_CRK | 437 | 441 | PF00017 | 0.469 |
LIG_SH2_PTP2 | 542 | 545 | PF00017 | 0.421 |
LIG_SH2_SRC | 542 | 545 | PF00017 | 0.343 |
LIG_SH2_SRC | 603 | 606 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.360 |
LIG_SH3_1 | 310 | 316 | PF00018 | 0.534 |
LIG_SH3_2 | 148 | 153 | PF14604 | 0.567 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.517 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.795 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.559 |
LIG_SH3_3 | 609 | 615 | PF00018 | 0.302 |
LIG_SUMO_SIM_par_1 | 282 | 288 | PF11976 | 0.359 |
LIG_TYR_ITIM | 15 | 20 | PF00017 | 0.689 |
LIG_TYR_ITIM | 414 | 419 | PF00017 | 0.443 |
LIG_TYR_ITIM | 465 | 470 | PF00017 | 0.462 |
LIG_TYR_ITIM | 601 | 606 | PF00017 | 0.327 |
LIG_UBA3_1 | 20 | 27 | PF00899 | 0.527 |
LIG_UBA3_1 | 211 | 217 | PF00899 | 0.438 |
LIG_WRC_WIRS_1 | 558 | 563 | PF05994 | 0.417 |
MOD_CDC14_SPxK_1 | 150 | 153 | PF00782 | 0.571 |
MOD_CDK_SPK_2 | 232 | 237 | PF00069 | 0.341 |
MOD_CDK_SPxK_1 | 147 | 153 | PF00069 | 0.569 |
MOD_CDK_SPxK_1 | 562 | 568 | PF00069 | 0.440 |
MOD_CDK_SPxxK_3 | 147 | 154 | PF00069 | 0.570 |
MOD_CDK_SPxxK_3 | 562 | 569 | PF00069 | 0.388 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.724 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.749 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.638 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.463 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.585 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.355 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.500 |
MOD_CMANNOS | 587 | 590 | PF00535 | 0.417 |
MOD_Cter_Amidation | 338 | 341 | PF01082 | 0.371 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.674 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.654 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.685 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.412 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.367 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.726 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.433 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.358 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.618 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.572 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.550 |
MOD_GlcNHglycan | 549 | 553 | PF01048 | 0.372 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.646 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.639 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.604 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.352 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.556 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.398 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.365 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.670 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.293 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.507 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.430 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.715 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.607 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.344 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.367 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.461 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.307 |
MOD_NEK2_2 | 131 | 136 | PF00069 | 0.489 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.296 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.394 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.480 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.421 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.365 |
MOD_PKB_1 | 175 | 183 | PF00069 | 0.547 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.624 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.429 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.664 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.615 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.355 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.386 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.618 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.453 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.414 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.451 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.737 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.333 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.744 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.452 |
MOD_ProDKin_1 | 562 | 568 | PF00069 | 0.354 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.319 |
MOD_SUMO_for_1 | 121 | 124 | PF00179 | 0.256 |
TRG_DiLeu_BaEn_1 | 207 | 212 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 418 | 423 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.312 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 442 | 444 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.286 |
TRG_ER_diArg_1 | 584 | 586 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.784 |
TRG_NLS_Bipartite_1 | 136 | 157 | PF00514 | 0.571 |
TRG_NLS_MonoExtC_3 | 339 | 344 | PF00514 | 0.427 |
TRG_NLS_MonoExtC_3 | 495 | 500 | PF00514 | 0.658 |
TRG_NLS_MonoExtN_4 | 151 | 157 | PF00514 | 0.745 |
TRG_NLS_MonoExtN_4 | 340 | 345 | PF00514 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYQ3 | Leptomonas seymouri | 59% | 97% |
A0A0S4KIC5 | Bodo saltans | 29% | 100% |
A0A0S4KP75 | Bodo saltans | 27% | 100% |
A0A1X0NS61 | Trypanosomatidae | 43% | 100% |
A0A1X0NSF5 | Trypanosomatidae | 26% | 100% |
A0A3Q8IDN6 | Leishmania donovani | 25% | 74% |
A0A3S5IR98 | Trypanosoma rangeli | 43% | 100% |
A4HEY9 | Leishmania braziliensis | 81% | 100% |
A4HEZ0 | Leishmania braziliensis | 25% | 100% |
A4I263 | Leishmania infantum | 100% | 100% |
A4I264 | Leishmania infantum | 25% | 74% |
C9ZRT4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AYB3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q959 | Leishmania major | 25% | 76% |
Q4Q960 | Leishmania major | 94% | 100% |
V5AUB9 | Trypanosoma cruzi | 26% | 100% |