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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HI85
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0005215 | transporter activity | 1 | 1 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.321 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.339 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.124 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.368 |
CLV_Separin_Metazoa | 87 | 91 | PF03568 | 0.402 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.522 |
DEG_SPOP_SBC_1 | 174 | 178 | PF00917 | 0.554 |
DOC_CKS1_1 | 442 | 447 | PF01111 | 0.440 |
DOC_MAPK_gen_1 | 273 | 281 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 337 | 345 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 416 | 425 | PF00069 | 0.292 |
DOC_MAPK_HePTP_8 | 126 | 138 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 129 | 138 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 317 | 324 | PF00069 | 0.283 |
DOC_MAPK_MEF2A_6 | 337 | 345 | PF00069 | 0.334 |
DOC_MAPK_NFAT4_5 | 338 | 346 | PF00069 | 0.280 |
DOC_PP1_RVXF_1 | 122 | 129 | PF00149 | 0.496 |
DOC_PP1_RVXF_1 | 436 | 443 | PF00149 | 0.334 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.432 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.435 |
LIG_14-3-3_CanoR_1 | 28 | 33 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 37 | 47 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 380 | 385 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 82 | 86 | PF00244 | 0.342 |
LIG_Clathr_ClatBox_1 | 117 | 121 | PF01394 | 0.476 |
LIG_CSL_BTD_1 | 5 | 8 | PF09270 | 0.459 |
LIG_deltaCOP1_diTrp_1 | 439 | 446 | PF00928 | 0.395 |
LIG_DLG_GKlike_1 | 28 | 36 | PF00625 | 0.279 |
LIG_EH1_1 | 82 | 90 | PF00400 | 0.286 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.329 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.332 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.205 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.485 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.257 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.428 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.333 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.330 |
LIG_GBD_Chelix_1 | 32 | 40 | PF00786 | 0.336 |
LIG_HP1_1 | 350 | 354 | PF01393 | 0.280 |
LIG_LIR_Apic_2 | 439 | 445 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 229 | 238 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 290 | 300 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 229 | 233 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.310 |
LIG_LYPXL_S_1 | 62 | 66 | PF13949 | 0.272 |
LIG_LYPXL_yS_3 | 63 | 66 | PF13949 | 0.285 |
LIG_NRBOX | 341 | 347 | PF00104 | 0.305 |
LIG_OCRL_FandH_1 | 260 | 272 | PF00620 | 0.285 |
LIG_Pex14_1 | 442 | 446 | PF04695 | 0.425 |
LIG_PTB_Apo_2 | 224 | 231 | PF02174 | 0.340 |
LIG_REV1ctd_RIR_1 | 258 | 268 | PF16727 | 0.305 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.282 |
LIG_SH2_SRC | 374 | 377 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 386 | 390 | PF00017 | 0.256 |
LIG_SH2_STAT3 | 141 | 144 | PF00017 | 0.460 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.615 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.485 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.595 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.486 |
LIG_SH3_5 | 137 | 141 | PF00018 | 0.376 |
LIG_SUMO_SIM_anti_2 | 115 | 121 | PF11976 | 0.337 |
LIG_SUMO_SIM_anti_2 | 399 | 405 | PF11976 | 0.262 |
LIG_SUMO_SIM_anti_2 | 84 | 90 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 318 | 323 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 347 | 356 | PF11976 | 0.246 |
LIG_SUMO_SIM_par_1 | 399 | 405 | PF11976 | 0.351 |
LIG_TYR_ITIM | 219 | 224 | PF00017 | 0.341 |
LIG_UBA3_1 | 106 | 111 | PF00899 | 0.431 |
LIG_UBA3_1 | 251 | 258 | PF00899 | 0.261 |
LIG_UBA3_1 | 341 | 349 | PF00899 | 0.261 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.642 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.628 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.590 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.205 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.261 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.423 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.325 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.510 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.286 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.312 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.246 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.370 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.496 |
MOD_Cter_Amidation | 271 | 274 | PF01082 | 0.391 |
MOD_DYRK1A_RPxSP_1 | 18 | 22 | PF00069 | 0.556 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.567 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.510 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.699 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.706 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.240 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.248 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.356 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.599 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.585 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.546 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.305 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.361 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.442 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.437 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.544 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.379 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.169 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.349 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.312 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.346 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.478 |
MOD_PK_1 | 419 | 425 | PF00069 | 0.416 |
MOD_PKA_1 | 28 | 34 | PF00069 | 0.490 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.319 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.285 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.495 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.496 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.342 |
MOD_PKB_1 | 436 | 444 | PF00069 | 0.345 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.392 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.324 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.375 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.385 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.368 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.389 |
MOD_Plk_2-3 | 72 | 78 | PF00069 | 0.342 |
MOD_Plk_2-3 | 81 | 87 | PF00069 | 0.327 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.648 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.246 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.267 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.266 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.288 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.484 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.396 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.531 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.513 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.449 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.436 |
MOD_SUMO_rev_2 | 121 | 131 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 21 | 31 | PF00179 | 0.553 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.266 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.324 |
TRG_NES_CRM1_1 | 314 | 327 | PF08389 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8R4 | Leptomonas seymouri | 70% | 90% |
A0A0S4J6G0 | Bodo saltans | 50% | 91% |
A0A1X0P1Z8 | Trypanosomatidae | 55% | 93% |
A0A3R7K7R6 | Trypanosoma rangeli | 54% | 95% |
A0A3S7X391 | Leishmania donovani | 79% | 100% |
A4I5G4 | Leishmania infantum | 79% | 100% |
C9ZQV0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 91% |
E9B0R2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
P33916 | Escherichia coli (strain K12) | 23% | 90% |
Q4Q7H1 | Leishmania major | 79% | 100% |
Q5HCL3 | Staphylococcus aureus (strain COL) | 23% | 83% |
Q6G5Z1 | Staphylococcus aureus (strain MSSA476) | 23% | 83% |
Q6GDC0 | Staphylococcus aureus (strain MRSA252) | 23% | 83% |
Q7A342 | Staphylococcus aureus (strain N315) | 23% | 83% |
Q87G35 | Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) | 24% | 82% |
Q897I2 | Clostridium tetani (strain Massachusetts / E88) | 21% | 100% |
Q8NUH8 | Staphylococcus aureus (strain MW2) | 23% | 83% |
Q8PSR0 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 21% | 80% |
Q8TQ05 | Methanosarcina acetivorans (strain ATCC 35395 / DSM 2834 / JCM 12185 / C2A) | 23% | 77% |
Q8XK20 | Clostridium perfringens (strain 13 / Type A) | 24% | 83% |
Q99QV7 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 23% | 83% |
V5BPK8 | Trypanosoma cruzi | 56% | 100% |