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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000228 | nuclear chromosome | 6 | 2 |
GO:0005694 | chromosome | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q1E2
Term | Name | Level | Count |
---|---|---|---|
GO:0000706 | meiotic DNA double-strand break processing | 3 | 2 |
GO:0000729 | DNA double-strand break processing | 5 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0007131 | reciprocal meiotic recombination | 3 | 2 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0035825 | homologous recombination | 6 | 2 |
GO:0042138 | meiotic DNA double-strand break formation | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0061982 | meiosis I cell cycle process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 2 |
GO:0140527 | reciprocal homologous recombination | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:1903046 | meiotic cell cycle process | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003916 | DNA topoisomerase activity | 3 | 11 |
GO:0003918 | DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) activity | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0000166 | nucleotide binding | 3 | 5 |
GO:0005524 | ATP binding | 5 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 5 |
GO:0030554 | adenyl nucleotide binding | 5 | 5 |
GO:0032553 | ribonucleotide binding | 3 | 5 |
GO:0032555 | purine ribonucleotide binding | 4 | 5 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 5 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 5 |
GO:0036094 | small molecule binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043168 | anion binding | 3 | 5 |
GO:0043169 | cation binding | 3 | 5 |
GO:0046872 | metal ion binding | 4 | 5 |
GO:0097367 | carbohydrate derivative binding | 2 | 5 |
GO:1901265 | nucleoside phosphate binding | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 423 | 427 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.443 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 408 | 410 | PF00082 | 0.528 |
CLV_PCSK_PC7_1 | 283 | 289 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.520 |
DEG_APCC_DBOX_1 | 282 | 290 | PF00400 | 0.367 |
DEG_APCC_DBOX_1 | 439 | 447 | PF00400 | 0.411 |
DEG_SCF_FBW7_1 | 418 | 425 | PF00400 | 0.446 |
DOC_CKS1_1 | 71 | 76 | PF01111 | 0.684 |
DOC_CYCLIN_yCln2_LP_2 | 191 | 197 | PF00134 | 0.579 |
DOC_MAPK_DCC_7 | 355 | 364 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 116 | 124 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 355 | 364 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 455 | 464 | PF00069 | 0.548 |
DOC_MAPK_JIP1_4 | 238 | 244 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 355 | 364 | PF00069 | 0.551 |
DOC_MAPK_NFAT4_5 | 357 | 365 | PF00069 | 0.533 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.588 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.547 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.520 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 109 | 115 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 231 | 240 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 265 | 270 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 44 | 51 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 440 | 444 | PF00244 | 0.448 |
LIG_Actin_WH2_2 | 394 | 410 | PF00022 | 0.497 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.665 |
LIG_CaM_IQ_9 | 401 | 417 | PF13499 | 0.555 |
LIG_Clathr_ClatBox_1 | 242 | 246 | PF01394 | 0.411 |
LIG_EH1_1 | 54 | 62 | PF00400 | 0.521 |
LIG_eIF4E_1 | 97 | 103 | PF01652 | 0.434 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.438 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.434 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.539 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.441 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.528 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.418 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.676 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.422 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.531 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.418 |
LIG_GBD_Chelix_1 | 183 | 191 | PF00786 | 0.484 |
LIG_LIR_Apic_2 | 141 | 147 | PF02991 | 0.583 |
LIG_LIR_Apic_2 | 321 | 327 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 266 | 277 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 338 | 348 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.733 |
LIG_LIR_Nem_3 | 54 | 58 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.734 |
LIG_LYPXL_yS_3 | 277 | 280 | PF13949 | 0.457 |
LIG_PDZ_Class_3 | 485 | 490 | PF00595 | 0.624 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.577 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.514 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.613 |
LIG_SH2_NCK_1 | 212 | 216 | PF00017 | 0.490 |
LIG_SH2_PTP2 | 299 | 302 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 212 | 216 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.448 |
LIG_SH2_STAT3 | 12 | 15 | PF00017 | 0.629 |
LIG_SH2_STAT3 | 56 | 59 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.419 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 193 | 199 | PF11976 | 0.545 |
LIG_SUMO_SIM_anti_2 | 21 | 27 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 187 | 193 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 196 | 201 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 241 | 246 | PF11976 | 0.374 |
LIG_WRC_WIRS_1 | 337 | 342 | PF05994 | 0.698 |
MOD_CDC14_SPxK_1 | 37 | 40 | PF00782 | 0.685 |
MOD_CDK_SPK_2 | 143 | 148 | PF00069 | 0.586 |
MOD_CDK_SPK_2 | 260 | 265 | PF00069 | 0.386 |
MOD_CDK_SPxK_1 | 34 | 40 | PF00069 | 0.663 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.762 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.451 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.559 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.663 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.477 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.515 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.547 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.524 |
MOD_GlcNHglycan | 199 | 203 | PF01048 | 0.498 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.553 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.719 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.622 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.581 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.628 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.600 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.647 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.483 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.464 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.473 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.716 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.575 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.566 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.414 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.511 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.605 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.724 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.535 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.396 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.539 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.338 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.571 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.644 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.604 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.601 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.634 |
MOD_OFUCOSY | 368 | 375 | PF10250 | 0.517 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.706 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.751 |
MOD_PIKK_1 | 391 | 397 | PF00454 | 0.613 |
MOD_PK_1 | 409 | 415 | PF00069 | 0.472 |
MOD_PKA_1 | 408 | 414 | PF00069 | 0.316 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.487 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.468 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.496 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.456 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.494 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.399 |
MOD_Plk_2-3 | 88 | 94 | PF00069 | 0.511 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.599 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.415 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.568 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.405 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.391 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.522 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.501 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.541 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.481 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.726 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.727 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.608 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.608 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.621 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.672 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.652 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.655 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.503 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.715 |
MOD_SUMO_for_1 | 458 | 461 | PF00179 | 0.499 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.746 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 97 | 100 | PF00400 | 0.352 |
TRG_NES_CRM1_1 | 14 | 30 | PF08389 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7M4 | Leptomonas seymouri | 40% | 100% |
A0A1X0NL58 | Trypanosomatidae | 30% | 100% |
A0A3R7LIJ3 | Trypanosoma rangeli | 31% | 100% |
A0A3S7XAZ9 | Leishmania donovani | 91% | 99% |
A4HPE4 | Leishmania braziliensis | 77% | 93% |
A4ICI5 | Leishmania infantum | 91% | 92% |
D0A3F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AT55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 99% |
V5BPV6 | Trypanosoma cruzi | 31% | 100% |