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. | yes | yes: 35 |
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: 24 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 13 |
GO:0043226 | organelle | 2 | 13 |
GO:0043227 | membrane-bounded organelle | 3 | 13 |
GO:0043229 | intracellular organelle | 3 | 13 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: Q4Q7A2
Term | Name | Level | Count |
---|---|---|---|
GO:0006091 | generation of precursor metabolites and energy | 3 | 13 |
GO:0006629 | lipid metabolic process | 3 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009056 | catabolic process | 2 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016042 | lipid catabolic process | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044248 | cellular catabolic process | 3 | 13 |
GO:0044281 | small molecule metabolic process | 2 | 13 |
GO:0044282 | small molecule catabolic process | 3 | 13 |
GO:0046950 | cellular ketone body metabolic process | 3 | 13 |
GO:0046952 | ketone body catabolic process | 4 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901568 | fatty acid derivative metabolic process | 4 | 13 |
GO:1901569 | fatty acid derivative catabolic process | 5 | 13 |
GO:1901575 | organic substance catabolic process | 3 | 13 |
GO:1902224 | ketone body metabolic process | 4 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0008260 | succinyl-CoA:3-oxo-acid CoA-transferase activity | 5 | 13 |
GO:0008410 | CoA-transferase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016782 | transferase activity, transferring sulphur-containing groups | 3 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.516 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.593 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.309 |
DEG_MDM2_SWIB_1 | 164 | 171 | PF02201 | 0.601 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.643 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.601 |
DOC_MAPK_DCC_7 | 229 | 238 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 278 | 284 | PF00069 | 0.514 |
DOC_MAPK_HePTP_8 | 282 | 294 | PF00069 | 0.601 |
DOC_MAPK_MEF2A_6 | 229 | 238 | PF00069 | 0.601 |
DOC_MAPK_MEF2A_6 | 285 | 294 | PF00069 | 0.601 |
DOC_MAPK_MEF2A_6 | 362 | 370 | PF00069 | 0.524 |
DOC_MAPK_NFAT4_5 | 285 | 293 | PF00069 | 0.601 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.601 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.700 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.610 |
LIG_14-3-3_CanoR_1 | 12 | 20 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 167 | 172 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.601 |
LIG_AP_GAE_1 | 66 | 72 | PF02883 | 0.460 |
LIG_CSL_BTD_1 | 385 | 388 | PF09270 | 0.601 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.608 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.603 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.576 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.559 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.453 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.502 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.618 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.525 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.576 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.373 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.532 |
LIG_Integrin_isoDGR_2 | 165 | 167 | PF01839 | 0.376 |
LIG_LIR_Apic_2 | 154 | 158 | PF02991 | 0.580 |
LIG_LIR_Apic_2 | 302 | 306 | PF02991 | 0.578 |
LIG_LIR_Apic_2 | 384 | 388 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 178 | 187 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.541 |
LIG_LIR_LC3C_4 | 400 | 403 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 178 | 182 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.460 |
LIG_MAD2 | 422 | 430 | PF02301 | 0.521 |
LIG_PDZ_Class_1 | 494 | 499 | PF00595 | 0.466 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.578 |
LIG_Pex14_2 | 97 | 101 | PF04695 | 0.586 |
LIG_PTB_Apo_2 | 86 | 93 | PF02174 | 0.490 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.567 |
LIG_SH2_PTP2 | 303 | 306 | PF00017 | 0.547 |
LIG_SH2_SRC | 303 | 306 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.524 |
LIG_SH3_1 | 143 | 149 | PF00018 | 0.471 |
LIG_SH3_1 | 488 | 494 | PF00018 | 0.417 |
LIG_SH3_2 | 146 | 151 | PF14604 | 0.471 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.471 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.547 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.508 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.382 |
LIG_SUMO_SIM_anti_2 | 408 | 413 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 407 | 413 | PF11976 | 0.538 |
LIG_TRAF2_1 | 469 | 472 | PF00917 | 0.544 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.727 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.536 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.485 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.460 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.615 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.512 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.344 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.362 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.346 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.291 |
MOD_GlcNHglycan | 375 | 379 | PF01048 | 0.358 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.621 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.381 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.325 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.506 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.582 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.557 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.509 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.265 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.268 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.499 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.581 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.600 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.551 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.531 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.513 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.535 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.601 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.586 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.554 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.524 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.590 |
MOD_PKB_1 | 10 | 18 | PF00069 | 0.234 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.524 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.449 |
MOD_Plk_2-3 | 466 | 472 | PF00069 | 0.503 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.610 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.584 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.592 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.373 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.547 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.460 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.506 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.524 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.610 |
MOD_SUMO_for_1 | 475 | 478 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 222 | 231 | PF00179 | 0.601 |
MOD_SUMO_rev_2 | 252 | 259 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 413 | 421 | PF00179 | 0.590 |
MOD_SUMO_rev_2 | 466 | 475 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 484 | 490 | PF00179 | 0.343 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P584 | Leptomonas seymouri | 53% | 100% |
A0A0N1I0F3 | Leptomonas seymouri | 47% | 100% |
A0A0S4JH09 | Bodo saltans | 53% | 100% |
A0A1X0NIU4 | Trypanosomatidae | 48% | 100% |
A0A1X0P425 | Trypanosomatidae | 51% | 100% |
A0A3Q8IC07 | Leishmania donovani | 81% | 100% |
A0A3Q8IMK1 | Leishmania donovani | 47% | 100% |
A0A3R7LBN6 | Trypanosoma rangeli | 51% | 100% |
A0A3S7X3G0 | Leishmania donovani | 95% | 100% |
A4HLU7 | Leishmania braziliensis | 46% | 100% |
A4I5L8 | Leishmania infantum | 81% | 100% |
A4I5L9 | Leishmania infantum | 95% | 100% |
B2GV06 | Rattus norvegicus | 49% | 96% |
D0A680 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AHQ2 | Leishmania infantum | 47% | 100% |
E9B0W3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
E9B0W4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9B473 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
F1CYZ5 | Acetobacterium woodii | 27% | 95% |
P37766 | Escherichia coli (strain K12) | 26% | 94% |
P55809 | Homo sapiens | 49% | 96% |
Q09450 | Caenorhabditis elegans | 48% | 96% |
Q29551 | Sus scrofa | 49% | 96% |
Q4Q3V3 | Leishmania major | 47% | 100% |
Q4Q7A3 | Leishmania major | 82% | 100% |
Q54JD9 | Dictyostelium discoideum | 50% | 98% |
Q5XIJ9 | Rattus norvegicus | 47% | 96% |
Q8X5X6 | Escherichia coli O157:H7 | 26% | 94% |
Q9BYC2 | Homo sapiens | 49% | 97% |
Q9D0K2 | Mus musculus | 49% | 96% |
Q9ESL0 | Mus musculus | 47% | 96% |
Q9JJN4 | Mus musculus | 47% | 96% |
Q9W058 | Drosophila melanogaster | 47% | 97% |
V5DQB8 | Trypanosoma cruzi | 49% | 100% |