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: 9 |
NetGPI | no | yes: 0, no: 9 |
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: A0A3S7WZC3
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 | 168 | 172 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.771 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.509 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.608 |
DEG_ODPH_VHL_1 | 37 | 49 | PF01847 | 0.516 |
DOC_ANK_TNKS_1 | 484 | 491 | PF00023 | 0.429 |
DOC_CKS1_1 | 40 | 45 | PF01111 | 0.481 |
DOC_CYCLIN_RxL_1 | 160 | 171 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 96 | 104 | PF00069 | 0.488 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.415 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.631 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 111 | 118 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 480 | 484 | PF00244 | 0.539 |
LIG_APCC_ABBA_1 | 245 | 250 | PF00400 | 0.525 |
LIG_APCC_ABBAyCdc20_2 | 63 | 69 | PF00400 | 0.609 |
LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.525 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.591 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.469 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.502 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.495 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.470 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.522 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.474 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.484 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.537 |
LIG_LIR_Gen_1 | 170 | 179 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 386 | 393 | PF02991 | 0.443 |
LIG_LIR_LC3C_4 | 299 | 304 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.450 |
LIG_MYND_1 | 311 | 315 | PF01753 | 0.517 |
LIG_MYND_1 | 35 | 39 | PF01753 | 0.558 |
LIG_Pex14_1 | 270 | 274 | PF04695 | 0.460 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.521 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 387 | 391 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.533 |
LIG_SH3_2 | 325 | 330 | PF14604 | 0.499 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.525 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.610 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.558 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.556 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.459 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.492 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.471 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 458 | 463 | PF11976 | 0.430 |
LIG_SUMO_SIM_anti_2 | 79 | 84 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 175 | 181 | PF11976 | 0.485 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.528 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.583 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.525 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.488 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.563 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.620 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.738 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.445 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.461 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.512 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.379 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.325 |
MOD_GlcNHglycan | 180 | 185 | PF01048 | 0.337 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.663 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.787 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.484 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.602 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.471 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.618 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.649 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.482 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.672 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.746 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.488 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.449 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.596 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.606 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.439 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.425 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.632 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.623 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.574 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.603 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.556 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.510 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.510 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.533 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.664 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.483 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.537 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.470 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.501 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.460 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.488 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.448 |
MOD_Plk_2-3 | 417 | 423 | PF00069 | 0.506 |
MOD_Plk_2-3 | 425 | 431 | PF00069 | 0.359 |
MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.466 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.576 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.460 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.308 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.441 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.663 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.552 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.553 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.415 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.583 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.616 |
TRG_DiLeu_BaLyEn_6 | 28 | 33 | PF01217 | 0.578 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.515 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 484 | 486 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.498 |
TRG_NES_CRM1_1 | 168 | 181 | PF08389 | 0.525 |
TRG_NES_CRM1_1 | 236 | 250 | PF08389 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 175 | 180 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I876 | Leptomonas seymouri | 54% | 100% |
A0A422NGJ8 | Trypanosoma rangeli | 29% | 100% |
A4HEG6 | Leishmania braziliensis | 77% | 98% |
A4I1M4 | Leishmania infantum | 99% | 100% |
C9ZK66 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AXQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 96% |
Q4Q9R3 | Leishmania major | 94% | 100% |
V5DIU3 | Trypanosoma cruzi | 33% | 100% |