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: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 |
GO:0000228 | nuclear chromosome | 6 | 1 |
Related structures:
AlphaFold database: A0A3S7XAZ9
Term | Name | Level | Count |
---|---|---|---|
GO:0000706 | meiotic DNA double-strand break processing | 3 | 1 |
GO:0000729 | DNA double-strand break processing | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006259 | DNA metabolic process | 4 | 6 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0007131 | reciprocal meiotic recombination | 3 | 1 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0035825 | homologous recombination | 6 | 1 |
GO:0042138 | meiotic DNA double-strand break formation | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0061982 | meiosis I cell cycle process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0140527 | reciprocal homologous recombination | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
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 | 426 | 430 | PF00656 | 0.596 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.736 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.736 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 411 | 413 | PF00082 | 0.528 |
CLV_PCSK_PC7_1 | 286 | 292 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.525 |
DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.379 |
DEG_APCC_DBOX_1 | 442 | 450 | PF00400 | 0.407 |
DEG_SCF_FBW7_1 | 167 | 172 | PF00400 | 0.421 |
DOC_CKS1_1 | 74 | 79 | PF01111 | 0.732 |
DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.589 |
DOC_MAPK_DCC_7 | 358 | 367 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 119 | 127 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 358 | 367 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 458 | 467 | PF00069 | 0.547 |
DOC_MAPK_JIP1_4 | 241 | 247 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 296 | 305 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 358 | 367 | PF00069 | 0.553 |
DOC_MAPK_NFAT4_5 | 360 | 368 | PF00069 | 0.534 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.592 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.677 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.766 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 443 | 447 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 47 | 54 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 65 | 70 | PF00244 | 0.407 |
LIG_Actin_WH2_2 | 397 | 413 | PF00022 | 0.496 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.649 |
LIG_BRCT_BRCA1_1 | 376 | 380 | PF00533 | 0.592 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.691 |
LIG_BRCT_BRCA1_1 | 489 | 493 | PF00533 | 0.436 |
LIG_CaM_IQ_9 | 404 | 420 | PF13499 | 0.552 |
LIG_CAP-Gly_1 | 486 | 493 | PF01302 | 0.412 |
LIG_Clathr_ClatBox_1 | 245 | 249 | PF01394 | 0.413 |
LIG_EH1_1 | 57 | 65 | PF00400 | 0.539 |
LIG_eIF4E_1 | 100 | 106 | PF01652 | 0.438 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.454 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.463 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.537 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.543 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.425 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.672 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.715 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.417 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.473 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.425 |
LIG_GBD_Chelix_1 | 186 | 194 | PF00786 | 0.493 |
LIG_LIR_Apic_2 | 144 | 150 | PF02991 | 0.599 |
LIG_LIR_Apic_2 | 324 | 330 | PF02991 | 0.648 |
LIG_LIR_Apic_2 | 97 | 103 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 269 | 275 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 75 | 85 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.782 |
LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.562 |
LIG_LYPXL_yS_3 | 280 | 283 | PF13949 | 0.494 |
LIG_PDZ_Class_3 | 488 | 493 | PF00595 | 0.607 |
LIG_Pex14_1 | 376 | 380 | PF04695 | 0.543 |
LIG_Pex14_2 | 30 | 34 | PF04695 | 0.571 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.496 |
LIG_SH2_CRK | 243 | 247 | PF00017 | 0.521 |
LIG_SH2_CRK | 270 | 274 | PF00017 | 0.380 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.716 |
LIG_SH2_NCK_1 | 215 | 219 | PF00017 | 0.503 |
LIG_SH2_PTP2 | 302 | 305 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 270 | 274 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.592 |
LIG_SH2_STAT3 | 59 | 62 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.432 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.448 |
LIG_SUMO_SIM_anti_2 | 196 | 202 | PF11976 | 0.557 |
LIG_SUMO_SIM_anti_2 | 24 | 30 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 199 | 204 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 244 | 249 | PF11976 | 0.381 |
LIG_WRC_WIRS_1 | 340 | 345 | PF05994 | 0.696 |
MOD_CDC14_SPxK_1 | 40 | 43 | PF00782 | 0.706 |
MOD_CDK_SPK_2 | 146 | 151 | PF00069 | 0.604 |
MOD_CDK_SPxK_1 | 37 | 43 | PF00069 | 0.685 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.487 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.747 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.602 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.655 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.507 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.485 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.467 |
MOD_GlcNHglycan | 202 | 206 | PF01048 | 0.516 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.439 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.597 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.717 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.617 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.675 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.615 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.669 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.584 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.619 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.514 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.472 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.495 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.749 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.507 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.661 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.767 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.604 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.540 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.420 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.645 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.383 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.599 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.565 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.633 |
MOD_OFUCOSY | 371 | 378 | PF10250 | 0.518 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.761 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.596 |
MOD_PK_1 | 412 | 418 | PF00069 | 0.470 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.490 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.476 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.476 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.394 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.533 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.446 |
MOD_Plk_2-3 | 91 | 97 | PF00069 | 0.522 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.583 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.419 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.395 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.509 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.498 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.545 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.450 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.679 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.609 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.643 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.633 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.711 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.758 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.685 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.768 |
MOD_SUMO_for_1 | 461 | 464 | PF00179 | 0.496 |
TRG_DiLeu_BaEn_1 | 24 | 29 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.744 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 458 | 461 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.713 |
TRG_NES_CRM1_1 | 17 | 33 | PF08389 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 448 | 452 | PF00026 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7M4 | Leptomonas seymouri | 41% | 100% |
A0A1X0NL58 | Trypanosomatidae | 31% | 100% |
A0A3R7LIJ3 | Trypanosoma rangeli | 31% | 100% |
A4HPE4 | Leishmania braziliensis | 79% | 100% |
A4ICI5 | Leishmania infantum | 100% | 100% |
D0A3F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AT55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q1E2 | Leishmania major | 91% | 100% |
V5BPV6 | Trypanosoma cruzi | 32% | 100% |