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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9AMI6
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 9 |
GO:0032259 | methylation | 2 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0008168 | methyltransferase activity | 4 | 10 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 10 |
GO:0008119 | thiopurine S-methyltransferase activity | 6 | 1 |
GO:0008172 | S-methyltransferase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.498 |
CLV_PCSK_FUR_1 | 6 | 10 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.288 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.406 |
DEG_APCC_DBOX_1 | 158 | 166 | PF00400 | 0.406 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.689 |
DEG_SCF_FBW7_2 | 415 | 422 | PF00400 | 0.623 |
DEG_SPOP_SBC_1 | 173 | 177 | PF00917 | 0.391 |
DOC_CKS1_1 | 386 | 391 | PF01111 | 0.505 |
DOC_MAPK_gen_1 | 310 | 321 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 379 | 387 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 6 | 14 | PF00069 | 0.663 |
DOC_PP2B_LxvP_1 | 417 | 420 | PF13499 | 0.618 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.339 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.528 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.300 |
DOC_PP4_MxPP_1 | 336 | 339 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.507 |
DOC_USP7_MATH_2 | 256 | 262 | PF00917 | 0.418 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.484 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.488 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.433 |
LIG_14-3-3_CanoR_1 | 171 | 181 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 198 | 207 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 403 | 408 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.586 |
LIG_Actin_WH2_2 | 17 | 32 | PF00022 | 0.651 |
LIG_Actin_WH2_2 | 364 | 381 | PF00022 | 0.528 |
LIG_BRCT_BRCA1_1 | 114 | 118 | PF00533 | 0.369 |
LIG_CaM_IQ_9 | 365 | 381 | PF13499 | 0.488 |
LIG_Clathr_ClatBox_1 | 318 | 322 | PF01394 | 0.552 |
LIG_deltaCOP1_diTrp_1 | 95 | 101 | PF00928 | 0.363 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.525 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.442 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.571 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.594 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.627 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.310 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.651 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.433 |
LIG_LIR_Apic_2 | 115 | 121 | PF02991 | 0.326 |
LIG_LIR_Apic_2 | 274 | 279 | PF02991 | 0.492 |
LIG_LIR_Apic_2 | 384 | 389 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 258 | 265 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 388 | 398 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.510 |
LIG_MLH1_MIPbox_1 | 114 | 118 | PF16413 | 0.369 |
LIG_MYND_1 | 415 | 419 | PF01753 | 0.672 |
LIG_Pex14_1 | 267 | 271 | PF04695 | 0.459 |
LIG_Pex14_2 | 64 | 68 | PF04695 | 0.300 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.334 |
LIG_SH2_CRK | 260 | 264 | PF00017 | 0.522 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.484 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 285 | 289 | PF00017 | 0.525 |
LIG_SH2_PTP2 | 386 | 389 | PF00017 | 0.522 |
LIG_SH2_PTP2 | 81 | 84 | PF00017 | 0.475 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.442 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.475 |
LIG_SH3_1 | 80 | 86 | PF00018 | 0.447 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.393 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.677 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.469 |
LIG_TRAF2_1 | 419 | 422 | PF00917 | 0.671 |
LIG_UBA3_1 | 161 | 167 | PF00899 | 0.323 |
LIG_UBA3_1 | 25 | 31 | PF00899 | 0.640 |
LIG_WRC_WIRS_1 | 148 | 153 | PF05994 | 0.422 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.371 |
MOD_CDK_SPxxK_3 | 218 | 225 | PF00069 | 0.442 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.454 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.505 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.539 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.666 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.609 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.407 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.459 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.599 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.501 |
MOD_Cter_Amidation | 281 | 284 | PF01082 | 0.284 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.595 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.407 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.723 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.678 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.394 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.423 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.505 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.532 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.352 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.476 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.706 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.624 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.362 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.461 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.672 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.542 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.542 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.535 |
MOD_PK_1 | 33 | 39 | PF00069 | 0.646 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.297 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.341 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.662 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.570 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.646 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.472 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.442 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.434 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.525 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.526 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.696 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.429 |
TRG_DiLeu_BaEn_1 | 72 | 77 | PF01217 | 0.409 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.436 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.663 |
TRG_NLS_MonoExtC_3 | 29 | 34 | PF00514 | 0.635 |
TRG_NLS_MonoExtN_4 | 28 | 34 | PF00514 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.289 |
TRG_PTS2 | 1 | 14 | PF00400 | 0.622 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4U9 | Leptomonas seymouri | 67% | 100% |
A0A0S4INW4 | Bodo saltans | 39% | 100% |
A0A1X0NF48 | Trypanosomatidae | 49% | 100% |
A0A3S5H690 | Leishmania donovani | 94% | 100% |
A4H5F4 | Leishmania braziliensis | 84% | 99% |
A4HTP9 | Leishmania infantum | 94% | 100% |
C9ZPF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
Q4QI53 | Leishmania major | 91% | 100% |