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: 20 |
NetGPI | no | yes: 0, no: 20 |
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: A4HEY9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 21 |
GO:0006259 | DNA metabolic process | 4 | 21 |
GO:0006281 | DNA repair | 5 | 21 |
GO:0006310 | DNA recombination | 5 | 21 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 21 |
GO:0006807 | nitrogen compound metabolic process | 2 | 21 |
GO:0006950 | response to stress | 2 | 21 |
GO:0006974 | DNA damage response | 4 | 21 |
GO:0008152 | metabolic process | 1 | 21 |
GO:0009987 | cellular process | 1 | 21 |
GO:0033554 | cellular response to stress | 3 | 21 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 21 |
GO:0043170 | macromolecule metabolic process | 3 | 21 |
GO:0044237 | cellular metabolic process | 2 | 21 |
GO:0044238 | primary metabolic process | 2 | 21 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 21 |
GO:0046483 | heterocycle metabolic process | 3 | 21 |
GO:0050896 | response to stimulus | 1 | 21 |
GO:0051716 | cellular response to stimulus | 2 | 21 |
GO:0071704 | organic substance metabolic process | 2 | 21 |
GO:0090304 | nucleic acid metabolic process | 4 | 21 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 21 |
GO:0003824 | catalytic activity | 1 | 21 |
GO:0003909 | DNA ligase activity | 4 | 21 |
GO:0003910 | DNA ligase (ATP) activity | 5 | 21 |
GO:0005488 | binding | 1 | 21 |
GO:0005524 | ATP binding | 5 | 21 |
GO:0016874 | ligase activity | 2 | 21 |
GO:0016886 | ligase activity, forming phosphoric ester bonds | 3 | 21 |
GO:0017076 | purine nucleotide binding | 4 | 21 |
GO:0030554 | adenyl nucleotide binding | 5 | 21 |
GO:0032553 | ribonucleotide binding | 3 | 21 |
GO:0032555 | purine ribonucleotide binding | 4 | 21 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 21 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 21 |
GO:0036094 | small molecule binding | 2 | 21 |
GO:0043167 | ion binding | 2 | 21 |
GO:0043168 | anion binding | 3 | 21 |
GO:0097159 | organic cyclic compound binding | 2 | 21 |
GO:0097367 | carbohydrate derivative binding | 2 | 21 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 21 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 21 |
GO:1901265 | nucleoside phosphate binding | 3 | 21 |
GO:1901363 | heterocyclic compound binding | 2 | 21 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.516 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 587 | 589 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.313 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.310 |
CLV_PCSK_PC1ET2_1 | 111 | 113 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.760 |
CLV_PCSK_PC1ET2_1 | 502 | 504 | PF00082 | 0.727 |
CLV_PCSK_PC1ET2_1 | 586 | 588 | PF00082 | 0.319 |
CLV_PCSK_PC7_1 | 26 | 32 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.328 |
DEG_APCC_DBOX_1 | 212 | 220 | PF00400 | 0.416 |
DEG_SCF_FBW7_1 | 382 | 387 | PF00400 | 0.423 |
DEG_SCF_FBW7_1 | 577 | 582 | PF00400 | 0.425 |
DOC_ANK_TNKS_1 | 623 | 630 | PF00023 | 0.562 |
DOC_CKS1_1 | 381 | 386 | PF01111 | 0.551 |
DOC_CYCLIN_RxL_1 | 277 | 286 | PF00134 | 0.381 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 213 | 219 | PF00134 | 0.409 |
DOC_MAPK_MEF2A_6 | 168 | 175 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 3 | 10 | PF00069 | 0.574 |
DOC_PP1_RVXF_1 | 254 | 261 | PF00149 | 0.461 |
DOC_PP1_RVXF_1 | 93 | 100 | PF00149 | 0.299 |
DOC_SPAK_OSR1_1 | 574 | 578 | PF12202 | 0.425 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.408 |
DOC_USP7_UBL2_3 | 221 | 225 | PF12436 | 0.370 |
DOC_USP7_UBL2_3 | 594 | 598 | PF12436 | 0.460 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 575 | 580 | PF00397 | 0.315 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.256 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.318 |
LIG_14-3-3_CanoR_1 | 181 | 187 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 25 | 32 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 481 | 487 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 530 | 535 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 574 | 578 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 588 | 594 | PF00244 | 0.230 |
LIG_Actin_WH2_2 | 431 | 449 | PF00022 | 0.504 |
LIG_APCC_Cbox_2 | 114 | 120 | PF00515 | 0.180 |
LIG_BRCT_BRCA1_1 | 402 | 406 | PF00533 | 0.554 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.589 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.456 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.518 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.432 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.573 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.561 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.482 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.299 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.377 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.725 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.319 |
LIG_LIR_Apic_2 | 378 | 384 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 203 | 211 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 331 | 342 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 542 | 551 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 563 | 569 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 603 | 614 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 417 | 423 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 554 | 560 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 563 | 567 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 603 | 609 | PF02991 | 0.312 |
LIG_MYND_1 | 316 | 320 | PF01753 | 0.417 |
LIG_NRBOX | 422 | 428 | PF00104 | 0.480 |
LIG_PDZ_Class_3 | 628 | 633 | PF00595 | 0.514 |
LIG_PDZ_Wminus1_1 | 631 | 633 | PF00595 | 0.494 |
LIG_Pex14_1 | 593 | 597 | PF04695 | 0.425 |
LIG_Pex14_2 | 560 | 564 | PF04695 | 0.279 |
LIG_REV1ctd_RIR_1 | 258 | 267 | PF16727 | 0.414 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.519 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.470 |
LIG_SH2_PTP2 | 545 | 548 | PF00017 | 0.400 |
LIG_SH2_SRC | 545 | 548 | PF00017 | 0.337 |
LIG_SH2_SRC | 606 | 609 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 402 | 406 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.356 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.298 |
LIG_SUMO_SIM_par_1 | 286 | 292 | PF11976 | 0.393 |
LIG_TYR_ITIM | 418 | 423 | PF00017 | 0.466 |
LIG_TYR_ITIM | 469 | 474 | PF00017 | 0.478 |
LIG_TYR_ITIM | 604 | 609 | PF00017 | 0.317 |
LIG_UBA3_1 | 215 | 221 | PF00899 | 0.467 |
LIG_WRC_WIRS_1 | 561 | 566 | PF05994 | 0.425 |
MOD_CDK_SPK_2 | 141 | 146 | PF00069 | 0.487 |
MOD_CDK_SPK_2 | 236 | 241 | PF00069 | 0.340 |
MOD_CDK_SPK_2 | 312 | 317 | PF00069 | 0.387 |
MOD_CDK_SPxK_1 | 565 | 571 | PF00069 | 0.445 |
MOD_CDK_SPxxK_3 | 565 | 572 | PF00069 | 0.398 |
MOD_CDK_SPxxK_3 | 88 | 95 | PF00069 | 0.312 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.662 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.705 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.461 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.389 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.214 |
MOD_CMANNOS | 590 | 593 | PF00535 | 0.425 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.668 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.677 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.627 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.620 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.464 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.650 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.477 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.370 |
MOD_GlcNHglycan | 385 | 389 | PF01048 | 0.445 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.476 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.655 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.625 |
MOD_GlcNHglycan | 552 | 556 | PF01048 | 0.365 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.635 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.582 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.599 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.375 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.551 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.615 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.434 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.461 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.532 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.490 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.288 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.441 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.664 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.686 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.369 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.324 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.380 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.458 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.279 |
MOD_NEK2_2 | 428 | 433 | PF00069 | 0.509 |
MOD_PK_1 | 348 | 354 | PF00069 | 0.462 |
MOD_PKA_1 | 159 | 165 | PF00069 | 0.600 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.647 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.667 |
MOD_PKA_1 | 502 | 508 | PF00069 | 0.670 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.487 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.499 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.557 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.407 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.510 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.600 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.740 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.438 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.376 |
MOD_PKB_1 | 179 | 187 | PF00069 | 0.547 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.446 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.481 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.649 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.639 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.389 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.408 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.290 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.374 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.362 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.457 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.416 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.712 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.330 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.682 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.420 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.363 |
MOD_ProDKin_1 | 575 | 581 | PF00069 | 0.315 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.256 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.318 |
MOD_SUMO_rev_2 | 505 | 512 | PF00179 | 0.475 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 422 | 427 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 606 | 609 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 476 | 478 | PF00400 | 0.283 |
TRG_ER_diArg_1 | 587 | 589 | PF00400 | 0.340 |
TRG_NLS_MonoExtC_3 | 498 | 503 | PF00514 | 0.708 |
TRG_Pf-PMV_PEXEL_1 | 280 | 284 | PF00026 | 0.376 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYQ3 | Leptomonas seymouri | 60% | 98% |
A0A0N1PAX3 | Leptomonas seymouri | 25% | 100% |
A0A0S4KIC5 | Bodo saltans | 32% | 100% |
A0A0S4KP75 | Bodo saltans | 29% | 100% |
A0A1X0NS61 | Trypanosomatidae | 46% | 100% |
A0A1X0NSF5 | Trypanosomatidae | 27% | 100% |
A0A3Q8IDN6 | Leishmania donovani | 27% | 100% |
A0A3Q8IDV4 | Leishmania donovani | 81% | 100% |
A0A3S5IR98 | Trypanosoma rangeli | 44% | 100% |
A4HEZ0 | Leishmania braziliensis | 27% | 100% |
A4I263 | Leishmania infantum | 81% | 100% |
A4I264 | Leishmania infantum | 27% | 100% |
C9ZRT4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AYB3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9AYB4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q959 | Leishmania major | 26% | 73% |
Q4Q960 | Leishmania major | 81% | 100% |
V5AUB9 | Trypanosoma cruzi | 27% | 100% |
V5DAB4 | Trypanosoma cruzi | 45% | 100% |