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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4HDT5
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0008817 | corrinoid adenosyltransferase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.463 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.214 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.415 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.214 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 127 | 129 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.397 |
CLV_PCSK_PC7_1 | 320 | 326 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.361 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.488 |
DOC_CKS1_1 | 254 | 259 | PF01111 | 0.469 |
DOC_CYCLIN_RxL_1 | 64 | 72 | PF00134 | 0.511 |
DOC_MAPK_gen_1 | 324 | 333 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 67 | 73 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 296 | 304 | PF00069 | 0.516 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.516 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.478 |
LIG_14-3-3_CanoR_1 | 11 | 19 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 128 | 137 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 3 | 10 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 346 | 351 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 354 | 361 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 36 | 43 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.526 |
LIG_Actin_WH2_2 | 209 | 226 | PF00022 | 0.516 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.469 |
LIG_BRCT_BRCA1_1 | 355 | 359 | PF00533 | 0.469 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.329 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.453 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.439 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.516 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.469 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.568 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.640 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.812 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.414 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.422 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.468 |
LIG_KLC1_Yacidic_2 | 85 | 90 | PF13176 | 0.516 |
LIG_LIR_Apic_2 | 85 | 91 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.461 |
LIG_MLH1_MIPbox_1 | 355 | 359 | PF16413 | 0.469 |
LIG_PCNA_PIPBox_1 | 330 | 339 | PF02747 | 0.516 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.298 |
LIG_SH2_GRB2like | 351 | 354 | PF00017 | 0.492 |
LIG_SH2_PTP2 | 88 | 91 | PF00017 | 0.516 |
LIG_SH2_SRC | 88 | 91 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.474 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.518 |
LIG_TYR_ITIM | 25 | 30 | PF00017 | 0.298 |
LIG_UBA3_1 | 103 | 108 | PF00899 | 0.516 |
MOD_CDK_SPK_2 | 6 | 11 | PF00069 | 0.473 |
MOD_CDK_SPxK_1 | 295 | 301 | PF00069 | 0.414 |
MOD_CDK_SPxxK_3 | 253 | 260 | PF00069 | 0.516 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.729 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.414 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.589 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.674 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.638 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.574 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.443 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.442 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.477 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.529 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.402 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.499 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.401 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.309 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.369 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.323 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.297 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.397 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.693 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.734 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.635 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.535 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.483 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.688 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.421 |
MOD_LATS_1 | 344 | 350 | PF00433 | 0.516 |
MOD_LATS_1 | 39 | 45 | PF00433 | 0.603 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.261 |
MOD_N-GLC_2 | 112 | 114 | PF02516 | 0.316 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.671 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.678 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.556 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.485 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.516 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.469 |
MOD_PKA_1 | 67 | 73 | PF00069 | 0.509 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.261 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.469 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.604 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.469 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.509 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.469 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.500 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.516 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.383 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.617 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.514 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.469 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.429 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.714 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.476 |
MOD_SUMO_rev_2 | 66 | 76 | PF00179 | 0.699 |
TRG_DiLeu_BaEn_2 | 274 | 280 | PF01217 | 0.434 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 30 | 33 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 334 | 339 | PF00026 | 0.214 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 67 | 72 | PF00026 | 0.417 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4KL87 | Bodo saltans | 43% | 100% |
A0A3Q8ID37 | Leishmania donovani | 83% | 100% |
A4I133 | Leishmania infantum | 83% | 100% |
E9AX70 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QAA6 | Leishmania major | 81% | 100% |