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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4H5F4
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 10 |
GO:0032259 | methylation | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
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 | 231 | 235 | PF00656 | 0.455 |
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.441 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.397 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.422 |
DEG_SCF_FBW7_2 | 411 | 418 | PF00400 | 0.647 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.395 |
DEG_SPOP_SBC_1 | 42 | 46 | PF00917 | 0.520 |
DOC_CKS1_1 | 412 | 417 | PF01111 | 0.578 |
DOC_MAPK_gen_1 | 306 | 317 | PF00069 | 0.566 |
DOC_MAPK_gen_1 | 375 | 383 | PF00069 | 0.628 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.646 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.368 |
DOC_PP4_FxxP_1 | 266 | 269 | PF00568 | 0.536 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.297 |
DOC_PP4_MxPP_1 | 332 | 335 | PF00568 | 0.496 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.500 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.498 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.653 |
DOC_USP7_UBL2_3 | 375 | 379 | PF12436 | 0.496 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.422 |
LIG_14-3-3_CanoR_1 | 195 | 204 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 399 | 404 | PF00244 | 0.653 |
LIG_Actin_WH2_2 | 17 | 32 | PF00022 | 0.678 |
LIG_Actin_WH2_2 | 360 | 377 | PF00022 | 0.538 |
LIG_BRCT_BRCA1_1 | 114 | 118 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.272 |
LIG_CaM_IQ_9 | 361 | 377 | PF13499 | 0.496 |
LIG_Clathr_ClatBox_1 | 314 | 318 | PF01394 | 0.536 |
LIG_deltaCOP1_diTrp_1 | 95 | 101 | PF00928 | 0.395 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.543 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.454 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.604 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.666 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.720 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.316 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.696 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.442 |
LIG_LIR_Apic_2 | 115 | 121 | PF02991 | 0.341 |
LIG_LIR_Apic_2 | 270 | 275 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 300 | 309 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.575 |
LIG_MLH1_MIPbox_1 | 114 | 118 | PF16413 | 0.396 |
LIG_MYND_1 | 411 | 415 | PF01753 | 0.717 |
LIG_Pex14_1 | 263 | 267 | PF04695 | 0.455 |
LIG_Pex14_2 | 64 | 68 | PF04695 | 0.297 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.339 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.477 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.498 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 281 | 285 | PF00017 | 0.536 |
LIG_SH2_PTP2 | 81 | 84 | PF00017 | 0.473 |
LIG_SH2_SRC | 316 | 319 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 281 | 285 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.453 |
LIG_SH2_STAT3 | 285 | 288 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.473 |
LIG_SH3_1 | 80 | 86 | PF00018 | 0.428 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.371 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.402 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.748 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.430 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.714 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.680 |
LIG_TYR_ITIM | 254 | 259 | PF00017 | 0.478 |
LIG_UBA3_1 | 25 | 31 | PF00899 | 0.667 |
LIG_UBA3_1 | 37 | 41 | PF00899 | 0.514 |
MOD_CDK_SPxxK_3 | 214 | 221 | PF00069 | 0.442 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.445 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.525 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.547 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.559 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.678 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.282 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.407 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.455 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.643 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.488 |
MOD_Cter_Amidation | 277 | 280 | PF01082 | 0.298 |
MOD_DYRK1A_RPxSP_1 | 168 | 172 | PF00069 | 0.420 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.614 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.660 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.436 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.282 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.455 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.533 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.494 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.695 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.683 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.379 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.486 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.688 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.585 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.582 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.536 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.523 |
MOD_PK_1 | 33 | 39 | PF00069 | 0.658 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.522 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.355 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.645 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.569 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.658 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.460 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.523 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.494 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.457 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.536 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.538 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.731 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.420 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 72 | 77 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 398 | 401 | PF00400 | 0.692 |
TRG_NLS_MonoExtC_3 | 29 | 34 | PF00514 | 0.688 |
TRG_NLS_MonoExtN_4 | 28 | 34 | PF00514 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 341 | 345 | PF00026 | 0.303 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4U9 | Leptomonas seymouri | 69% | 100% |
A0A0S4INW4 | Bodo saltans | 39% | 100% |
A0A1X0NF48 | Trypanosomatidae | 51% | 100% |
A0A3S5H690 | Leishmania donovani | 86% | 99% |
A4HTP9 | Leishmania infantum | 86% | 99% |
C9ZPF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AMI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
Q4QI53 | Leishmania major | 84% | 100% |
V5BIU8 | Trypanosoma cruzi | 50% | 100% |