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: A4ICI5
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 | 466 | 470 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.382 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 451 | 453 | PF00082 | 0.492 |
CLV_PCSK_PC7_1 | 326 | 332 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.442 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.306 |
DEG_APCC_DBOX_1 | 482 | 490 | PF00400 | 0.348 |
DEG_SCF_FBW7_1 | 207 | 212 | PF00400 | 0.354 |
DEG_SCF_FBW7_1 | 8 | 15 | PF00400 | 0.421 |
DOC_CKS1_1 | 114 | 119 | PF01111 | 0.603 |
DOC_CYCLIN_yCln2_LP_2 | 234 | 240 | PF00134 | 0.450 |
DOC_MAPK_DCC_7 | 398 | 407 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 159 | 167 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 398 | 407 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 498 | 507 | PF00069 | 0.438 |
DOC_MAPK_JIP1_4 | 281 | 287 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 336 | 345 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.418 |
DOC_MAPK_NFAT4_5 | 400 | 408 | PF00069 | 0.403 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.422 |
DOC_PP2B_LxvP_1 | 145 | 148 | PF13499 | 0.456 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.498 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.638 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.516 |
LIG_14-3-3_CanoR_1 | 105 | 110 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 152 | 158 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 25 | 35 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 483 | 487 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 87 | 94 | PF00244 | 0.473 |
LIG_Actin_WH2_2 | 437 | 453 | PF00022 | 0.474 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.543 |
LIG_BRCT_BRCA1_1 | 426 | 430 | PF00533 | 0.623 |
LIG_BRCT_BRCA1_1 | 529 | 533 | PF00533 | 0.385 |
LIG_CaM_IQ_9 | 444 | 460 | PF13499 | 0.422 |
LIG_CAP-Gly_1 | 526 | 533 | PF01302 | 0.351 |
LIG_Clathr_ClatBox_1 | 285 | 289 | PF01394 | 0.355 |
LIG_EH1_1 | 97 | 105 | PF00400 | 0.398 |
LIG_eIF4E_1 | 140 | 146 | PF01652 | 0.370 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.553 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.382 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.402 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.441 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.488 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.421 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.392 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.348 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.516 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.356 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.368 |
LIG_GBD_Chelix_1 | 226 | 234 | PF00786 | 0.446 |
LIG_LIR_Apic_2 | 137 | 143 | PF02991 | 0.468 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 364 | 370 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 115 | 125 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 309 | 315 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 309 | 313 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 381 | 386 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.452 |
LIG_LYPXL_yS_3 | 320 | 323 | PF13949 | 0.466 |
LIG_MYND_1 | 12 | 16 | PF01753 | 0.422 |
LIG_PDZ_Class_3 | 528 | 533 | PF00595 | 0.573 |
LIG_Pex14_1 | 416 | 420 | PF04695 | 0.449 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.421 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.551 |
LIG_SH2_CRK | 140 | 144 | PF00017 | 0.489 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.490 |
LIG_SH2_CRK | 310 | 314 | PF00017 | 0.516 |
LIG_SH2_NCK_1 | 255 | 259 | PF00017 | 0.452 |
LIG_SH2_PTP2 | 342 | 345 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.357 |
LIG_SH2_STAT3 | 55 | 58 | PF00017 | 0.484 |
LIG_SH2_STAT3 | 99 | 102 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.399 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.553 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.412 |
LIG_SUMO_SIM_anti_2 | 236 | 242 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 64 | 70 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 239 | 244 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 284 | 289 | PF11976 | 0.319 |
LIG_WRC_WIRS_1 | 380 | 385 | PF05994 | 0.588 |
MOD_CDC14_SPxK_1 | 80 | 83 | PF00782 | 0.544 |
MOD_CDK_SPK_2 | 186 | 191 | PF00069 | 0.448 |
MOD_CDK_SPxK_1 | 77 | 83 | PF00069 | 0.530 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.476 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.447 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.630 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.390 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.524 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.444 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.412 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.456 |
MOD_GlcNHglycan | 242 | 246 | PF01048 | 0.473 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.378 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.508 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.666 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.553 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.590 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.607 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.627 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.631 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.565 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.622 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.475 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.482 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.452 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.493 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.588 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.449 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.622 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.512 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.503 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.356 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.517 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.293 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.566 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.720 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.585 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.603 |
MOD_OFUCOSY | 411 | 418 | PF10250 | 0.397 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.620 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.562 |
MOD_PK_1 | 452 | 458 | PF00069 | 0.372 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.390 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.439 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.441 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.464 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.510 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.336 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.469 |
MOD_Plk_2-3 | 131 | 137 | PF00069 | 0.416 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.587 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.563 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.360 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.343 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.491 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.457 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.412 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.456 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.623 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.453 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.593 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.506 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.649 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.724 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.592 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 501 | 504 | PF00179 | 0.456 |
TRG_DiLeu_BaEn_1 | 64 | 69 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.637 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 498 | 501 | PF00400 | 0.539 |
TRG_NES_CRM1_1 | 57 | 73 | PF08389 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 25 | 30 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 488 | 492 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7M4 | Leptomonas seymouri | 41% | 100% |
A0A1X0NL58 | Trypanosomatidae | 31% | 100% |
A0A3R7LIJ3 | Trypanosoma rangeli | 31% | 100% |
A0A3S7XAZ9 | Leishmania donovani | 100% | 100% |
A4HPE4 | Leishmania braziliensis | 79% | 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 | 31% | 100% |