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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005794 | Golgi apparatus | 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 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HF63
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006893 | Golgi to plasma membrane transport | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0034067 | protein localization to Golgi apparatus | 6 | 1 |
GO:0043001 | Golgi to plasma membrane protein transport | 5 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0061951 | establishment of protein localization to plasma membrane | 5 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0072659 | protein localization to plasma membrane | 5 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:0098876 | vesicle-mediated transport to the plasma membrane | 4 | 1 |
GO:1990778 | protein localization to cell periphery | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0003924 | GTPase activity | 7 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005525 | GTP binding | 5 | 8 |
GO:0016462 | pyrophosphatase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 8 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 8 |
GO:0019001 | guanyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 329 | 333 | PF00656 | 0.528 |
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.413 |
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.522 |
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.479 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.661 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.304 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.360 |
DEG_APCC_DBOX_1 | 252 | 260 | PF00400 | 0.360 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.502 |
DEG_SPOP_SBC_1 | 88 | 92 | PF00917 | 0.526 |
DOC_CDC14_PxL_1 | 265 | 273 | PF14671 | 0.300 |
DOC_CKS1_1 | 13 | 18 | PF01111 | 0.503 |
DOC_CKS1_1 | 40 | 45 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 98 | 109 | PF00134 | 0.478 |
DOC_CYCLIN_yCln2_LP_2 | 104 | 107 | PF00134 | 0.448 |
DOC_CYCLIN_yCln2_LP_2 | 260 | 266 | PF00134 | 0.376 |
DOC_MAPK_gen_1 | 121 | 129 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 121 | 129 | PF00069 | 0.483 |
DOC_PP2B_LxvP_1 | 104 | 107 | PF13499 | 0.448 |
DOC_PP2B_LxvP_1 | 160 | 163 | PF13499 | 0.523 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.531 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.662 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.321 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.491 |
LIG_14-3-3_CanoR_1 | 83 | 88 | PF00244 | 0.531 |
LIG_Actin_WH2_2 | 216 | 231 | PF00022 | 0.219 |
LIG_BRCT_BRCA1_1 | 183 | 187 | PF00533 | 0.415 |
LIG_EVH1_1 | 160 | 164 | PF00568 | 0.546 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.416 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.651 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.410 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.391 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.279 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.411 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.360 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.350 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.357 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.654 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.726 |
LIG_GBD_Chelix_1 | 215 | 223 | PF00786 | 0.376 |
LIG_LIR_Apic_2 | 11 | 16 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 17 | 23 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 184 | 195 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.543 |
LIG_LIR_LC3C_4 | 139 | 143 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 302 | 306 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.546 |
LIG_NRBOX | 255 | 261 | PF00104 | 0.360 |
LIG_PCNA_PIPBox_1 | 198 | 207 | PF02747 | 0.360 |
LIG_PCNA_yPIPBox_3 | 193 | 205 | PF02747 | 0.360 |
LIG_PCNA_yPIPBox_3 | 237 | 249 | PF02747 | 0.219 |
LIG_PDZ_Class_3 | 405 | 410 | PF00595 | 0.464 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.300 |
LIG_PTB_Apo_2 | 297 | 304 | PF02174 | 0.328 |
LIG_PTB_Apo_2 | 7 | 14 | PF02174 | 0.542 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.445 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.355 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 131 | 135 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.410 |
LIG_SH2_STAT3 | 208 | 211 | PF00017 | 0.247 |
LIG_SH2_STAT3 | 304 | 307 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.492 |
LIG_SH3_1 | 229 | 235 | PF00018 | 0.219 |
LIG_SH3_2 | 232 | 237 | PF14604 | 0.219 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.658 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.445 |
LIG_SUMO_SIM_par_1 | 139 | 144 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 376 | 381 | PF11976 | 0.416 |
LIG_TRAF2_1 | 287 | 290 | PF00917 | 0.328 |
LIG_TYR_ITIM | 129 | 134 | PF00017 | 0.446 |
LIG_UBA3_1 | 270 | 276 | PF00899 | 0.219 |
LIG_UBA3_1 | 33 | 38 | PF00899 | 0.416 |
MOD_CDC14_SPxK_1 | 234 | 237 | PF00782 | 0.219 |
MOD_CDC14_SPxK_1 | 350 | 353 | PF00782 | 0.518 |
MOD_CDK_SPxK_1 | 231 | 237 | PF00069 | 0.219 |
MOD_CDK_SPxK_1 | 347 | 353 | PF00069 | 0.518 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.546 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.569 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.364 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.378 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.363 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.740 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.677 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.735 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.530 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.312 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.350 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.357 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.680 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.324 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.522 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.521 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.668 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.537 |
MOD_GlcNHglycan | 379 | 383 | PF01048 | 0.398 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.633 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.574 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.577 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.243 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.376 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.606 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.690 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.466 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.635 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.541 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.646 |
MOD_LATS_1 | 81 | 87 | PF00433 | 0.528 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.360 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.576 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.316 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.653 |
MOD_NEK2_2 | 371 | 376 | PF00069 | 0.487 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.622 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.360 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.250 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.697 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.471 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.474 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.416 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.293 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.662 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.305 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.376 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.358 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.471 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.416 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.473 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.483 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.510 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.464 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.353 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.596 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.597 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.496 |
MOD_SUMO_rev_2 | 238 | 248 | PF00179 | 0.315 |
MOD_SUMO_rev_2 | 71 | 80 | PF00179 | 0.523 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_1 | 290 | 295 | PF01217 | 0.219 |
TRG_DiLeu_BaEn_2 | 34 | 40 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.311 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 193 | 198 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.219 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTD1 | Leptomonas seymouri | 55% | 100% |
A0A3Q8ICC5 | Leishmania donovani | 71% | 100% |
A4I2E6 | Leishmania infantum | 72% | 100% |
C9ZX62 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AYJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4Q8X3 | Leishmania major | 70% | 97% |