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: A4HPE4
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 | 459 | 463 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.496 |
CLV_PCSK_PC7_1 | 320 | 326 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.438 |
DEG_APCC_DBOX_1 | 184 | 192 | PF00400 | 0.366 |
DEG_APCC_DBOX_1 | 475 | 483 | PF00400 | 0.345 |
DOC_CKS1_1 | 108 | 113 | PF01111 | 0.605 |
DOC_CKS1_1 | 458 | 463 | PF01111 | 0.429 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.433 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 234 | PF00134 | 0.447 |
DOC_MAPK_DCC_7 | 391 | 400 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 153 | 161 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 391 | 400 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 491 | 500 | PF00069 | 0.438 |
DOC_MAPK_JIP1_4 | 275 | 281 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 391 | 400 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 55 | 64 | PF00069 | 0.256 |
DOC_MAPK_NFAT4_5 | 393 | 401 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 482 | 489 | PF00149 | 0.245 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.458 |
DOC_PP4_FxxP_1 | 181 | 184 | PF00568 | 0.504 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.503 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.588 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 196 | 205 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 268 | 274 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 476 | 480 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 81 | 88 | PF00244 | 0.478 |
LIG_Actin_WH2_2 | 439 | 457 | PF00022 | 0.353 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.451 |
LIG_BRCT_BRCA1_1 | 372 | 376 | PF00533 | 0.672 |
LIG_BRCT_BRCA1_1 | 409 | 413 | PF00533 | 0.550 |
LIG_CaM_IQ_9 | 437 | 453 | PF13499 | 0.430 |
LIG_Clathr_ClatBox_1 | 279 | 283 | PF01394 | 0.348 |
LIG_EH1_1 | 91 | 99 | PF00400 | 0.405 |
LIG_eIF4E_1 | 134 | 140 | PF01652 | 0.377 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.575 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.474 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.412 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.534 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.399 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.394 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.579 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.465 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.371 |
LIG_GBD_Chelix_1 | 220 | 228 | PF00786 | 0.448 |
LIG_LIR_Apic_2 | 131 | 137 | PF02991 | 0.478 |
LIG_LIR_Apic_2 | 179 | 184 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 157 | 166 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 303 | 314 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 91 | 95 | PF02991 | 0.456 |
LIG_LYPXL_yS_3 | 112 | 115 | PF13949 | 0.505 |
LIG_LYPXL_yS_3 | 314 | 317 | PF13949 | 0.464 |
LIG_PCNA_yPIPBox_3 | 50 | 61 | PF02747 | 0.270 |
LIG_Pex14_1 | 409 | 413 | PF04695 | 0.455 |
LIG_Pex14_2 | 64 | 68 | PF04695 | 0.444 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.393 |
LIG_SH2_PTP2 | 306 | 309 | PF00017 | 0.230 |
LIG_SH2_PTP2 | 336 | 339 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 49 | 52 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 93 | 96 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.406 |
LIG_SH3_1 | 455 | 461 | PF00018 | 0.388 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.388 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.423 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.581 |
LIG_SUMO_SIM_anti_2 | 157 | 163 | PF11976 | 0.253 |
LIG_SUMO_SIM_anti_2 | 230 | 236 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 58 | 64 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 224 | 230 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 233 | 238 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 278 | 283 | PF11976 | 0.311 |
LIG_TRFH_1 | 6 | 10 | PF08558 | 0.462 |
MOD_CDC14_SPxK_1 | 183 | 186 | PF00782 | 0.321 |
MOD_CDC14_SPxK_1 | 74 | 77 | PF00782 | 0.571 |
MOD_CDK_SPK_2 | 180 | 185 | PF00069 | 0.455 |
MOD_CDK_SPxK_1 | 180 | 186 | PF00069 | 0.306 |
MOD_CDK_SPxK_1 | 71 | 77 | PF00069 | 0.548 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.429 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.470 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.470 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.487 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.650 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.548 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.428 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.476 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.597 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.554 |
MOD_GlcNHglycan | 236 | 240 | PF01048 | 0.482 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.370 |
MOD_GlcNHglycan | 260 | 264 | PF01048 | 0.356 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.572 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.591 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.643 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.637 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.551 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.614 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.593 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.651 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.480 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.549 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.433 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.447 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.616 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.555 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.528 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.462 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.566 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.606 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.573 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.512 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.302 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.570 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.599 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.505 |
MOD_NEK2_2 | 148 | 153 | PF00069 | 0.399 |
MOD_NEK2_2 | 176 | 181 | PF00069 | 0.536 |
MOD_OFUCOSY | 404 | 411 | PF10250 | 0.407 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.392 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.648 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.584 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.685 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.459 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.474 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.527 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.333 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.476 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.721 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.348 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.435 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.596 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.356 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.436 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.559 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.376 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.332 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.503 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.420 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.313 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.464 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.553 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.623 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.439 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.463 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.622 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.411 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.595 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.677 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.744 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.487 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.609 |
MOD_SUMO_for_1 | 494 | 497 | PF00179 | 0.461 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 110 | 115 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 183 | 188 | PF01217 | 0.313 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.650 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 467 | 469 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 491 | 494 | PF00400 | 0.536 |
TRG_NES_CRM1_1 | 51 | 67 | PF08389 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 185 | 190 | PF00026 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 481 | 485 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7M4 | Leptomonas seymouri | 40% | 100% |
A0A1X0NL58 | Trypanosomatidae | 30% | 100% |
A0A3R7LIJ3 | Trypanosoma rangeli | 30% | 100% |
A0A3S7XAZ9 | Leishmania donovani | 79% | 100% |
A4ICI5 | Leishmania infantum | 79% | 99% |
D0A3F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AT55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q1E2 | Leishmania major | 77% | 100% |
V5BPV6 | Trypanosoma cruzi | 30% | 100% |