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: 1, no: 21 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0020023 | kinetoplast | 2 | 1 |
Related structures:
AlphaFold database: A4HF09
Term | Name | Level | Count |
---|---|---|---|
GO:0001516 | prostaglandin biosynthetic process | 8 | 4 |
GO:0006082 | organic acid metabolic process | 3 | 4 |
GO:0006629 | lipid metabolic process | 3 | 4 |
GO:0006631 | fatty acid metabolic process | 4 | 4 |
GO:0006633 | fatty acid biosynthetic process | 5 | 4 |
GO:0006636 | unsaturated fatty acid biosynthetic process | 6 | 4 |
GO:0006690 | icosanoid metabolic process | 6 | 4 |
GO:0006692 | prostanoid metabolic process | 6 | 4 |
GO:0006693 | prostaglandin metabolic process | 7 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0008610 | lipid biosynthetic process | 4 | 4 |
GO:0009058 | biosynthetic process | 2 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016053 | organic acid biosynthetic process | 4 | 4 |
GO:0019752 | carboxylic acid metabolic process | 5 | 4 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 4 |
GO:0033559 | unsaturated fatty acid metabolic process | 5 | 4 |
GO:0043436 | oxoacid metabolic process | 4 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044249 | cellular biosynthetic process | 3 | 4 |
GO:0044255 | cellular lipid metabolic process | 3 | 4 |
GO:0044281 | small molecule metabolic process | 2 | 4 |
GO:0044283 | small molecule biosynthetic process | 3 | 4 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 4 |
GO:0046456 | icosanoid biosynthetic process | 6 | 4 |
GO:0046457 | prostanoid biosynthetic process | 7 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:0072330 | monocarboxylic acid biosynthetic process | 6 | 4 |
GO:1901576 | organic substance biosynthetic process | 3 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 20 |
GO:0015035 | protein-disulfide reductase activity | 3 | 18 |
GO:0015036 | disulfide oxidoreductase activity | 4 | 18 |
GO:0016491 | oxidoreductase activity | 2 | 18 |
GO:0016667 | oxidoreductase activity, acting on a sulfur group of donors | 3 | 18 |
GO:0097573 | obsolete glutathione oxidoreductase activity | 4 | 18 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 18 |
GO:0016671 | oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor | 4 | 5 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016860 | intramolecular oxidoreductase activity | 3 | 11 |
GO:0019153 | protein-disulfide reductase (glutathione) activity | 4 | 5 |
GO:0050220 | prostaglandin-E synthase activity | 4 | 11 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 1 |
GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | 4 | 1 |
GO:0036134 | 12-hydroxyheptadecatrienoic acid synthase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.325 |
CLV_C14_Caspase3-7 | 279 | 283 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.419 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.701 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.602 |
DOC_CDC14_PxL_1 | 155 | 163 | PF14671 | 0.308 |
DOC_CKS1_1 | 243 | 248 | PF01111 | 0.325 |
DOC_CYCLIN_yCln2_LP_2 | 118 | 124 | PF00134 | 0.271 |
DOC_CYCLIN_yCln2_LP_2 | 196 | 202 | PF00134 | 0.356 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.287 |
DOC_MAPK_RevD_3 | 140 | 154 | PF00069 | 0.432 |
DOC_PP1_RVXF_1 | 109 | 115 | PF00149 | 0.308 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.355 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.478 |
LIG_14-3-3_CanoR_1 | 101 | 110 | PF00244 | 0.396 |
LIG_Actin_WH2_2 | 45 | 61 | PF00022 | 0.421 |
LIG_deltaCOP1_diTrp_1 | 216 | 222 | PF00928 | 0.362 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.318 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.521 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.508 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.626 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.353 |
LIG_LIR_Apic_2 | 240 | 246 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 134 | 145 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 240 | 249 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 48 | 55 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 76 | 84 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.514 |
LIG_PCNA_PIPBox_1 | 326 | 335 | PF02747 | 0.414 |
LIG_PCNA_yPIPBox_3 | 326 | 340 | PF02747 | 0.428 |
LIG_PDZ_Class_2 | 392 | 397 | PF00595 | 0.634 |
LIG_PTB_Apo_2 | 228 | 235 | PF02174 | 0.379 |
LIG_PTB_Apo_2 | 248 | 255 | PF02174 | 0.214 |
LIG_PTB_Phospho_1 | 248 | 254 | PF10480 | 0.230 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.256 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.313 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.371 |
LIG_SH2_GRB2like | 249 | 252 | PF00017 | 0.333 |
LIG_SH2_GRB2like | 78 | 81 | PF00017 | 0.361 |
LIG_SH2_NCK_1 | 137 | 141 | PF00017 | 0.269 |
LIG_SH2_PTP2 | 243 | 246 | PF00017 | 0.315 |
LIG_SH2_SRC | 137 | 140 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 202 | 206 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.361 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.232 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.326 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.596 |
LIG_TRAF2_1 | 383 | 386 | PF00917 | 0.466 |
LIG_TRFH_1 | 155 | 159 | PF08558 | 0.299 |
LIG_TYR_ITIM | 113 | 118 | PF00017 | 0.301 |
LIG_TYR_ITIM | 130 | 135 | PF00017 | 0.242 |
LIG_WRC_WIRS_1 | 329 | 334 | PF05994 | 0.538 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.463 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.545 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.329 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.392 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.690 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.625 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.485 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.545 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.385 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.520 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.545 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.552 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.594 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.334 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.452 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.482 |
MOD_GlcNHglycan | 43 | 47 | PF01048 | 0.536 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.344 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.292 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.386 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.675 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.483 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.667 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.525 |
MOD_LATS_1 | 365 | 371 | PF00433 | 0.555 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.682 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.505 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.290 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.570 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.321 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.717 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.511 |
MOD_PK_1 | 367 | 373 | PF00069 | 0.551 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.518 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.419 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.445 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.288 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.333 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.386 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.535 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.583 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.548 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.313 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.493 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.478 |
MOD_SUMO_for_1 | 124 | 127 | PF00179 | 0.271 |
MOD_SUMO_rev_2 | 106 | 113 | PF00179 | 0.395 |
TRG_DiLeu_BaEn_2 | 327 | 333 | PF01217 | 0.510 |
TRG_DiLeu_BaLyEn_6 | 113 | 118 | PF01217 | 0.290 |
TRG_DiLeu_BaLyEn_6 | 270 | 275 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.257 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 270 | 273 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 273 | 277 | PF00026 | 0.217 |
TRG_Pf-PMV_PEXEL_1 | 310 | 314 | PF00026 | 0.219 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.562 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HS46 | Leptomonas seymouri | 26% | 100% |
A0A0N1ILY8 | Leptomonas seymouri | 60% | 100% |
A0A0S4IXT4 | Bodo saltans | 23% | 100% |
A0A0S4JV60 | Bodo saltans | 32% | 100% |
A0A1X0NND6 | Trypanosomatidae | 28% | 100% |
A0A1X0NTT0 | Trypanosomatidae | 39% | 100% |
A0A3S7WT83 | Leishmania donovani | 27% | 100% |
A0A3S7WZV5 | Leishmania donovani | 84% | 100% |
A0A422MZ79 | Trypanosoma rangeli | 41% | 100% |
A0A422N3R5 | Trypanosoma rangeli | 26% | 100% |
A4H7W8 | Leishmania braziliensis | 28% | 100% |
A4HW95 | Leishmania infantum | 27% | 100% |
A4I288 | Leishmania infantum | 84% | 100% |
C9ZRQ5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZSR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9APZ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AYD3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q940 | Leishmania major | 83% | 100% |
Q4QFI5 | Leishmania major | 27% | 100% |
V5AYZ4 | Trypanosoma cruzi | 40% | 100% |
V5DC17 | Trypanosoma cruzi | 26% | 100% |