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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005794 | Golgi apparatus | 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 |
Related structures:
AlphaFold database: E9AH03
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 2 |
GO:0006605 | protein targeting | 5 | 2 |
GO:0006612 | protein targeting to membrane | 5 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006897 | endocytosis | 5 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018198 | peptidyl-cysteine modification | 6 | 2 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 2 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 2 |
GO:0018345 | protein palmitoylation | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 15 |
GO:0016409 | palmitoyltransferase activity | 5 | 15 |
GO:0016417 | S-acyltransferase activity | 5 | 15 |
GO:0016740 | transferase activity | 2 | 15 |
GO:0016746 | acyltransferase activity | 3 | 15 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 15 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 15 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 15 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.737 |
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.653 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.547 |
CLV_PCSK_FUR_1 | 24 | 28 | PF00082 | 0.318 |
CLV_PCSK_FUR_1 | 286 | 290 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.361 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.402 |
CLV_PCSK_PC7_1 | 257 | 263 | PF00082 | 0.438 |
CLV_PCSK_PC7_1 | 288 | 294 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.321 |
DEG_APCC_DBOX_1 | 97 | 105 | PF00400 | 0.541 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.651 |
DOC_MAPK_MEF2A_6 | 210 | 217 | PF00069 | 0.260 |
DOC_MAPK_MEF2A_6 | 64 | 71 | PF00069 | 0.236 |
DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.372 |
DOC_PP2B_LxvP_1 | 365 | 368 | PF13499 | 0.666 |
DOC_SPAK_OSR1_1 | 64 | 68 | PF12202 | 0.236 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.750 |
DOC_USP7_UBL2_3 | 256 | 260 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.288 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.799 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 198 | 208 | PF00244 | 0.263 |
LIG_14-3-3_CanoR_1 | 7 | 15 | PF00244 | 0.631 |
LIG_APCC_ABBA_1 | 239 | 244 | PF00400 | 0.488 |
LIG_BIR_III_4 | 327 | 331 | PF00653 | 0.659 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.680 |
LIG_BRCT_BRCA1_1 | 77 | 81 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_2 | 77 | 83 | PF00533 | 0.229 |
LIG_CaM_IQ_9 | 183 | 199 | PF13499 | 0.417 |
LIG_EH1_1 | 183 | 191 | PF00400 | 0.350 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.442 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.272 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.691 |
LIG_GBD_Chelix_1 | 67 | 75 | PF00786 | 0.304 |
LIG_IRF3_LxIS_1 | 33 | 40 | PF10401 | 0.494 |
LIG_IRF3_LxIS_1 | 65 | 72 | PF10401 | 0.460 |
LIG_LIR_Apic_2 | 17 | 22 | PF02991 | 0.552 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.288 |
LIG_LIR_Apic_2 | 28 | 33 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 249 | 255 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 40 | 50 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 78 | 89 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.804 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.332 |
LIG_Pex14_1 | 15 | 19 | PF04695 | 0.543 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.449 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.288 |
LIG_SH2_NCK_1 | 356 | 360 | PF00017 | 0.698 |
LIG_SH2_SRC | 242 | 245 | PF00017 | 0.528 |
LIG_SH2_SRC | 251 | 254 | PF00017 | 0.480 |
LIG_SH2_SRC | 30 | 33 | PF00017 | 0.548 |
LIG_SH2_SRC | 364 | 367 | PF00017 | 0.709 |
LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.463 |
LIG_SH2_STAT3 | 184 | 187 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 267 | 270 | PF00017 | 0.667 |
LIG_SH2_STAT3 | 89 | 92 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.699 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.664 |
LIG_SH3_1 | 19 | 25 | PF00018 | 0.529 |
LIG_SH3_2 | 22 | 27 | PF14604 | 0.510 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.525 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.786 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.363 |
LIG_SUMO_SIM_par_1 | 66 | 73 | PF11976 | 0.312 |
LIG_WRC_WIRS_1 | 164 | 169 | PF05994 | 0.407 |
MOD_CDC14_SPxK_1 | 207 | 210 | PF00782 | 0.236 |
MOD_CDK_SPxK_1 | 204 | 210 | PF00069 | 0.236 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.414 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.695 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.690 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.779 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.772 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.480 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.494 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.741 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.431 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.332 |
MOD_GlcNHglycan | 327 | 331 | PF01048 | 0.557 |
MOD_GlcNHglycan | 341 | 345 | PF01048 | 0.581 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.480 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.339 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.659 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.449 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.747 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.764 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.295 |
MOD_N-GLC_2 | 153 | 155 | PF02516 | 0.263 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.328 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.469 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.507 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.353 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.295 |
MOD_OFUCOSY | 149 | 155 | PF10250 | 0.263 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.253 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.719 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.731 |
MOD_PK_1 | 133 | 139 | PF00069 | 0.504 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.494 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.685 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.402 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.392 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.371 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.288 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.799 |
MOD_SUMO_rev_2 | 10 | 18 | PF00179 | 0.633 |
MOD_SUMO_rev_2 | 269 | 279 | PF00179 | 0.664 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.730 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.749 |
TRG_NLS_MonoCore_2 | 285 | 290 | PF00514 | 0.654 |
TRG_NLS_MonoExtN_4 | 286 | 291 | PF00514 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.471 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3T7 | Leptomonas seymouri | 66% | 97% |
A0A0S4IT15 | Bodo saltans | 24% | 100% |
A0A0S4J1K8 | Bodo saltans | 24% | 86% |
A0A0S4JRL4 | Bodo saltans | 23% | 100% |
A0A1X0NUX2 | Trypanosomatidae | 49% | 100% |
A0A3R7RC91 | Trypanosoma rangeli | 43% | 100% |
A0A3S5H6J6 | Leishmania donovani | 31% | 100% |
A0A3S7WX91 | Leishmania donovani | 100% | 100% |
A4H6N2 | Leishmania braziliensis | 33% | 75% |
A4HCH5 | Leishmania braziliensis | 74% | 99% |
A4HD15 | Leishmania braziliensis | 24% | 100% |
B3DN87 | Arabidopsis thaliana | 24% | 100% |
C9ZSP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A148 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
D0A7D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 75% |
E7EZI4 | Danio rerio | 27% | 92% |
E7F4Z4 | Danio rerio | 27% | 68% |
E9AVW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
F1R013 | Danio rerio | 24% | 100% |
P0C7U3 | Homo sapiens | 26% | 100% |
P59268 | Mus musculus | 26% | 100% |
Q14AK4 | Mus musculus | 27% | 100% |
Q4QBL2 | Leishmania major | 93% | 100% |
Q4QGX1 | Leishmania major | 29% | 100% |
Q6DR03 | Arabidopsis thaliana | 26% | 70% |
Q8R0N9 | Mus musculus | 28% | 81% |
Q8VYP5 | Arabidopsis thaliana | 26% | 100% |
Q8WTX9 | Homo sapiens | 27% | 81% |
Q9H8X9 | Homo sapiens | 26% | 96% |
Q9M306 | Arabidopsis thaliana | 26% | 83% |
Q9SB58 | Arabidopsis thaliana | 24% | 97% |
V5B8P9 | Trypanosoma cruzi | 47% | 100% |
V5BWI0 | Trypanosoma cruzi | 27% | 100% |