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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905202 | methylcrotonoyl-CoA carboxylase complex | 3 | 1 |
Related structures:
AlphaFold database: A4H6I5
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006520 | amino acid metabolic process | 3 | 12 |
GO:0006551 | leucine metabolic process | 5 | 12 |
GO:0006552 | leucine catabolic process | 6 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009063 | amino acid catabolic process | 4 | 12 |
GO:0009081 | branched-chain amino acid metabolic process | 4 | 12 |
GO:0009083 | branched-chain amino acid catabolic process | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016054 | organic acid catabolic process | 4 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0044282 | small molecule catabolic process | 3 | 12 |
GO:0046395 | carboxylic acid catabolic process | 5 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 12 |
GO:1901606 | alpha-amino acid catabolic process | 5 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004485 | methylcrotonoyl-CoA carboxylase activity | 5 | 8 |
GO:0016421 | CoA carboxylase activity | 4 | 8 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016885 | ligase activity, forming carbon-carbon bonds | 3 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 40 | 44 | PF00656 | 0.332 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.432 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.162 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.164 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.382 |
DEG_APCC_DBOX_1 | 422 | 430 | PF00400 | 0.162 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.391 |
DOC_CYCLIN_yCln2_LP_2 | 30 | 36 | PF00134 | 0.571 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 422 | 429 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 226 | 235 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 389 | 397 | PF00069 | 0.285 |
DOC_MAPK_MEF2A_6 | 422 | 429 | PF00069 | 0.236 |
DOC_PP1_RVXF_1 | 213 | 219 | PF00149 | 0.164 |
DOC_PP2B_PxIxI_1 | 462 | 468 | PF00149 | 0.236 |
DOC_PP4_FxxP_1 | 491 | 494 | PF00568 | 0.236 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.296 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.515 |
DOC_USP7_UBL2_3 | 531 | 535 | PF12436 | 0.251 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.357 |
LIG_14-3-3_CanoR_1 | 21 | 30 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 276 | 282 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 497 | 501 | PF00244 | 0.251 |
LIG_Actin_WH2_2 | 505 | 520 | PF00022 | 0.382 |
LIG_CaM_IQ_9 | 525 | 540 | PF13499 | 0.162 |
LIG_EVH1_2 | 266 | 270 | PF00568 | 0.270 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.270 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.245 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.288 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.236 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.236 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.236 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.242 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.369 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.236 |
LIG_LIR_Gen_1 | 370 | 379 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 486 | 496 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 7 | 16 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 7 | 11 | PF02991 | 0.446 |
LIG_Pex14_2 | 213 | 217 | PF04695 | 0.236 |
LIG_Pex14_2 | 485 | 489 | PF04695 | 0.236 |
LIG_Rb_pABgroove_1 | 331 | 339 | PF01858 | 0.382 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.511 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.440 |
LIG_SH2_SRC | 244 | 247 | PF00017 | 0.263 |
LIG_SH2_SRC | 441 | 444 | PF00017 | 0.270 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 405 | 409 | PF00017 | 0.236 |
LIG_SH2_STAP1 | 8 | 12 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.438 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.382 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.464 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.236 |
LIG_SUMO_SIM_par_1 | 508 | 513 | PF11976 | 0.255 |
LIG_SUMO_SIM_par_1 | 79 | 84 | PF11976 | 0.314 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.190 |
LIG_TRAF2_1 | 69 | 72 | PF00917 | 0.440 |
LIG_TYR_ITIM | 6 | 11 | PF00017 | 0.382 |
LIG_WW_1 | 334 | 337 | PF00397 | 0.330 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.425 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.451 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.196 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.383 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.415 |
MOD_Cter_Amidation | 437 | 440 | PF01082 | 0.295 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.276 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.236 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.282 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.251 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.254 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.176 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.471 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.423 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.251 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.323 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.162 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.251 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.236 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.298 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.236 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.257 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.382 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.286 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.287 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.201 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.295 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.330 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.236 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.429 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.330 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.298 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.417 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.162 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.251 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.251 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.336 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.236 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.236 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.386 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.361 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.236 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.250 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.268 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.243 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.294 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.345 |
MOD_SUMO_rev_2 | 323 | 333 | PF00179 | 0.314 |
MOD_SUMO_rev_2 | 368 | 378 | PF00179 | 0.238 |
TRG_DiLeu_BaEn_2 | 340 | 346 | PF01217 | 0.251 |
TRG_DiLeu_BaLyEn_6 | 104 | 109 | PF01217 | 0.298 |
TRG_DiLeu_BaLyEn_6 | 422 | 427 | PF01217 | 0.236 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.236 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.162 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4K5 | Leptomonas seymouri | 32% | 100% |
A0A0N1IIF0 | Leptomonas seymouri | 83% | 87% |
A0A0S4IW40 | Bodo saltans | 65% | 85% |
A0A0S4J7G9 | Bodo saltans | 32% | 100% |
A0A1X0NV46 | Trypanosomatidae | 70% | 93% |
A0A3Q8I921 | Leishmania donovani | 93% | 100% |
A0A3R7M923 | Trypanosoma rangeli | 70% | 93% |
A0A3S7X171 | Leishmania donovani | 32% | 100% |
A4HG89 | Leishmania braziliensis | 33% | 100% |
A4HUX0 | Leishmania infantum | 93% | 100% |
D0A7I1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 95% |
E9ANK4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AZL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
I3R7F1 | Haloferax mediterranei (strain ATCC 33500 / DSM 1411 / JCM 8866 / NBRC 14739 / NCIMB 2177 / R-4) | 33% | 100% |
I6YDK7 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 60% | 100% |
O31825 | Bacillus subtilis (strain 168) | 38% | 100% |
O53578 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 29% | 100% |
O54028 | Propionigenium modestum | 33% | 100% |
O86318 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 48% | 100% |
P05166 | Homo sapiens | 31% | 100% |
P07633 | Rattus norvegicus | 32% | 100% |
P34385 | Caenorhabditis elegans | 57% | 95% |
P53002 | Mycobacterium leprae (strain TN) | 31% | 100% |
P53003 | Saccharopolyspora erythraea (strain ATCC 11635 / DSM 40517 / JCM 4748 / NBRC 13426 / NCIMB 8594 / NRRL 2338) | 34% | 100% |
P54541 | Bacillus subtilis (strain 168) | 33% | 100% |
P63408 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 31% | 100% |
P79384 | Sus scrofa | 32% | 100% |
P9WQH4 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 31% | 100% |
P9WQH5 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 31% | 100% |
P9WQH6 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 32% | 100% |
P9WQH7 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 32% | 100% |
Q06101 | Rhodococcus erythropolis | 33% | 100% |
Q06700 | Acidaminococcus fermentans (strain ATCC 25085 / DSM 20731 / CCUG 9996 / CIP 106432 / VR4) | 28% | 99% |
Q168G2 | Roseobacter denitrificans (strain ATCC 33942 / OCh 114) | 32% | 100% |
Q2TBR0 | Bos taurus | 32% | 100% |
Q3J4E3 | Cereibacter sphaeroides (strain ATCC 17023 / DSM 158 / JCM 6121 / CCUG 31486 / LMG 2827 / NBRC 12203 / NCIMB 8253 / ATH 2.4.1.) | 34% | 100% |
Q3ULD5 | Mus musculus | 61% | 100% |
Q4Q8M1 | Leishmania major | 32% | 100% |
Q4QH21 | Leishmania major | 93% | 100% |
Q57079 | Veillonella parvula | 32% | 100% |
Q5XIT9 | Rattus norvegicus | 61% | 100% |
Q8GBW6 | Propionibacterium freudenreichii subsp. shermanii | 34% | 100% |
Q8T2J9 | Dictyostelium discoideum | 60% | 98% |
Q99MN9 | Mus musculus | 31% | 100% |
Q9HCC0 | Homo sapiens | 59% | 100% |
Q9LDD8 | Arabidopsis thaliana | 56% | 99% |
Q9V9A7 | Drosophila melanogaster | 59% | 100% |
V5BWB7 | Trypanosoma cruzi | 69% | 94% |