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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 26 |
NetGPI | no | yes: 0, no: 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0016020 | membrane | 2 | 9 |
GO:0005739 | mitochondrion | 5 | 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 |
Related structures:
AlphaFold database: Q4QAE9
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006631 | fatty acid metabolic process | 4 | 1 |
GO:0006633 | fatty acid biosynthetic process | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016053 | organic acid biosynthetic process | 4 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0030497 | fatty acid elongation | 6 | 1 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0004312 | fatty acid synthase activity | 5 | 3 |
GO:0004316 | 3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity | 5 | 3 |
GO:0016491 | oxidoreductase activity | 2 | 3 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 3 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016746 | acyltransferase activity | 3 | 3 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.527 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.565 |
DEG_APCC_DBOX_1 | 127 | 135 | PF00400 | 0.454 |
DEG_APCC_DBOX_1 | 6 | 14 | PF00400 | 0.581 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.706 |
DEG_SPOP_SBC_1 | 237 | 241 | PF00917 | 0.204 |
DEG_SPOP_SBC_1 | 43 | 47 | PF00917 | 0.756 |
DOC_CYCLIN_RxL_1 | 24 | 33 | PF00134 | 0.594 |
DOC_CYCLIN_yCln2_LP_2 | 129 | 135 | PF00134 | 0.364 |
DOC_MAPK_DCC_7 | 397 | 406 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 127 | 135 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 299 | 308 | PF00069 | 0.241 |
DOC_MAPK_gen_1 | 388 | 395 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 127 | 135 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 301 | 310 | PF00069 | 0.318 |
DOC_MAPK_NFAT4_5 | 128 | 136 | PF00069 | 0.361 |
DOC_PP1_RVXF_1 | 250 | 256 | PF00149 | 0.241 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.364 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.281 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.556 |
DOC_USP7_UBL2_3 | 496 | 500 | PF12436 | 0.405 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 163 | 167 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 252 | 256 | PF00244 | 0.244 |
LIG_14-3-3_CanoR_1 | 325 | 334 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 369 | 376 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 397 | 404 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.321 |
LIG_APCC_ABBAyCdc20_2 | 170 | 176 | PF00400 | 0.289 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.592 |
LIG_CSL_BTD_1 | 129 | 132 | PF09270 | 0.283 |
LIG_eIF4E_1 | 194 | 200 | PF01652 | 0.270 |
LIG_eIF4E_1 | 466 | 472 | PF01652 | 0.321 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.413 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.277 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.272 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.366 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.258 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.679 |
LIG_LIR_Apic_2 | 143 | 148 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 178 | 184 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 254 | 261 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.323 |
LIG_Pex14_2 | 310 | 314 | PF04695 | 0.242 |
LIG_PTB_Apo_2 | 384 | 391 | PF02174 | 0.386 |
LIG_PTB_Apo_2 | 459 | 466 | PF02174 | 0.300 |
LIG_PTB_Phospho_1 | 384 | 390 | PF10480 | 0.381 |
LIG_PTB_Phospho_1 | 459 | 465 | PF10480 | 0.302 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.323 |
LIG_SH2_GRB2like | 145 | 148 | PF00017 | 0.235 |
LIG_SH2_NCK_1 | 113 | 117 | PF00017 | 0.629 |
LIG_SH2_NCK_1 | 154 | 158 | PF00017 | 0.492 |
LIG_SH2_SRC | 145 | 148 | PF00017 | 0.235 |
LIG_SH2_STAP1 | 136 | 140 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 466 | 470 | PF00017 | 0.258 |
LIG_SH2_STAT3 | 260 | 263 | PF00017 | 0.329 |
LIG_SH2_STAT3 | 380 | 383 | PF00017 | 0.233 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.216 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.416 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.376 |
LIG_SUMO_SIM_anti_2 | 262 | 268 | PF11976 | 0.243 |
LIG_SUMO_SIM_anti_2 | 279 | 285 | PF11976 | 0.287 |
LIG_TYR_ITSM | 176 | 183 | PF00017 | 0.326 |
LIG_UBA3_1 | 320 | 326 | PF00899 | 0.233 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.618 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.728 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.347 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.752 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.695 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.315 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.625 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.647 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.623 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.394 |
MOD_Cter_Amidation | 167 | 170 | PF01082 | 0.644 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.440 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.448 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.383 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.332 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.499 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.593 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.566 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.406 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.464 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.545 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.526 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.449 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.447 |
MOD_GlcNHglycan | 99 | 103 | PF01048 | 0.344 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.303 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.400 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.311 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.674 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.254 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.659 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.640 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.639 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.392 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.359 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.645 |
MOD_N-GLC_2 | 453 | 455 | PF02516 | 0.471 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.580 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.407 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.698 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.679 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.232 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.424 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.340 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.346 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.330 |
MOD_NEK2_2 | 86 | 91 | PF00069 | 0.756 |
MOD_PIKK_1 | 445 | 451 | PF00454 | 0.257 |
MOD_PKA_1 | 325 | 331 | PF00069 | 0.320 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.340 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.244 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.241 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.416 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.254 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.714 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.618 |
MOD_Plk_2-3 | 215 | 221 | PF00069 | 0.255 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.421 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.270 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.410 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.253 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.324 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.359 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.640 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.585 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.628 |
MOD_SUMO_rev_2 | 477 | 485 | PF00179 | 0.307 |
MOD_SUMO_rev_2 | 89 | 98 | PF00179 | 0.659 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.266 |
TRG_DiLeu_BaEn_2 | 216 | 222 | PF01217 | 0.334 |
TRG_DiLeu_BaLyEn_6 | 25 | 30 | PF01217 | 0.593 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 27 | 29 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.694 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2S5 | Leptomonas seymouri | 29% | 100% |
A0A0N0P2S7 | Leptomonas seymouri | 80% | 99% |
A0A0N1HZ81 | Leptomonas seymouri | 32% | 91% |
A0A0S4IWT0 | Bodo saltans | 46% | 100% |
A0A0S4IZG2 | Bodo saltans | 30% | 100% |
A0A0S4J1I6 | Bodo saltans | 31% | 100% |
A0A1X0NVT8 | Trypanosomatidae | 64% | 100% |
A0A3Q8ID46 | Leishmania donovani | 92% | 100% |
A0A3Q8IM89 | Leishmania donovani | 29% | 100% |
A0A3R7K071 | Trypanosoma rangeli | 32% | 100% |
A0A3R7N7S2 | Trypanosoma rangeli | 26% | 100% |
A0A3S5H7D5 | Leishmania donovani | 34% | 100% |
A0A3S7WQY1 | Leishmania donovani | 27% | 100% |
A0A422N2B6 | Trypanosoma rangeli | 62% | 100% |
A4H5Z1 | Leishmania braziliensis | 24% | 100% |
A4HDP2 | Leishmania braziliensis | 33% | 100% |
A4HDP3 | Leishmania braziliensis | 87% | 100% |
A4HMN7 | Leishmania braziliensis | 28% | 100% |
A4HUB6 | Leishmania infantum | 27% | 100% |
C9ZWC0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
C9ZWC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZZF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AF39 | Leishmania major | 29% | 100% |
E9AH88 | Leishmania infantum | 34% | 100% |
E9AH89 | Leishmania infantum | 92% | 100% |
E9AHV6 | Leishmania infantum | 29% | 100% |
E9AN15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AX26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AX27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B694 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4QAF0 | Leishmania major | 34% | 100% |
Q4QHL1 | Leishmania major | 27% | 100% |
Q6UX07 | Homo sapiens | 27% | 100% |
Q803A8 | Danio rerio | 27% | 100% |
Q92247 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 25% | 100% |
V5BAF4 | Trypanosoma cruzi | 62% | 100% |
V5BJC7 | Trypanosoma cruzi | 25% | 100% |