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:0005737 | cytoplasm | 2 | 1 |
GO:0016604 | nuclear body | 2 | 1 |
GO:0031422 | RecQ family helicase-topoisomerase III complex | 3 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A4HEG6
Term | Name | Level | Count |
---|---|---|---|
GO:0000712 | resolution of meiotic recombination intermediates | 4 | 1 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0061982 | meiosis I cell cycle process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004519 | endonuclease activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 176 | 180 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.775 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.629 |
DEG_APCC_DBOX_1 | 107 | 115 | PF00400 | 0.405 |
DEG_ODPH_VHL_1 | 37 | 49 | PF01847 | 0.651 |
DOC_CKS1_1 | 159 | 164 | PF01111 | 0.405 |
DOC_CYCLIN_RxL_1 | 103 | 115 | PF00134 | 0.510 |
DOC_CYCLIN_RxL_1 | 168 | 179 | PF00134 | 0.487 |
DOC_CYCLIN_RxL_1 | 447 | 455 | PF00134 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 309 | 315 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 103 | 111 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 487 | 496 | PF00069 | 0.318 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.645 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.738 |
LIG_14-3-3_CanoR_1 | 450 | 455 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.547 |
LIG_APCC_ABBA_1 | 254 | 259 | PF00400 | 0.534 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.469 |
LIG_BIR_III_2 | 143 | 147 | PF00653 | 0.405 |
LIG_BRCT_BRCA1_1 | 177 | 181 | PF00533 | 0.562 |
LIG_CtBP_PxDLS_1 | 206 | 212 | PF00389 | 0.516 |
LIG_EH1_1 | 84 | 92 | PF00400 | 0.227 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.405 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.405 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.541 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.487 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.516 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.556 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.484 |
LIG_LIR_Gen_1 | 178 | 187 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 388 | 395 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 388 | 392 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.415 |
LIG_MYND_1 | 35 | 39 | PF01753 | 0.645 |
LIG_SH2_CRK | 198 | 202 | PF00017 | 0.542 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.541 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 389 | 393 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.623 |
LIG_SH3_1 | 281 | 287 | PF00018 | 0.532 |
LIG_SH3_2 | 327 | 332 | PF14604 | 0.575 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.562 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.679 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.599 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.602 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.606 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.535 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.524 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.624 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.586 |
LIG_SUMO_SIM_anti_2 | 491 | 498 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 86 | 91 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 450 | 455 | PF11976 | 0.331 |
LIG_UBA3_1 | 90 | 97 | PF00899 | 0.405 |
MOD_CDK_SPK_2 | 402 | 407 | PF00069 | 0.444 |
MOD_CDK_SPxK_1 | 409 | 415 | PF00069 | 0.516 |
MOD_CDK_SPxxK_3 | 409 | 416 | PF00069 | 0.555 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.591 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.562 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.579 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.764 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.548 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.555 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.690 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.328 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.589 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.386 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.350 |
MOD_GlcNHglycan | 188 | 193 | PF01048 | 0.362 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.334 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.481 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.706 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.522 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.485 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.687 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.563 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.637 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.683 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.733 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.511 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.615 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.778 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.721 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.514 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.586 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.542 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.624 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.544 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.641 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.466 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.718 |
MOD_PK_1 | 66 | 72 | PF00069 | 0.539 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.697 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.628 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.470 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.548 |
MOD_PKB_1 | 64 | 72 | PF00069 | 0.543 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.659 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.496 |
MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.620 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.553 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.448 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.496 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.405 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.361 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.740 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.624 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.455 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.569 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.617 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.735 |
TRG_DiLeu_BaEn_1 | 425 | 430 | PF01217 | 0.403 |
TRG_DiLeu_BaLyEn_6 | 159 | 164 | PF01217 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 28 | 33 | PF01217 | 0.750 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 106 | 109 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.552 |
TRG_NES_CRM1_1 | 176 | 189 | PF08389 | 0.562 |
TRG_NES_CRM1_1 | 245 | 259 | PF08389 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 171 | 176 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 183 | 188 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 407 | 411 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I876 | Leptomonas seymouri | 53% | 100% |
A0A0S4ILE1 | Bodo saltans | 25% | 100% |
A0A3S7WZC3 | Leishmania donovani | 77% | 100% |
A0A422NGJ8 | Trypanosoma rangeli | 29% | 100% |
A4I1M4 | Leishmania infantum | 77% | 100% |
C9ZK66 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AXQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q9R3 | Leishmania major | 78% | 98% |
V5DIU3 | Trypanosoma cruzi | 32% | 100% |