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: Q4QI53
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:0008119 | thiopurine S-methyltransferase activity | 6 | 2 |
GO:0008168 | methyltransferase activity | 4 | 10 |
GO:0008172 | S-methyltransferase activity | 5 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.508 |
CLV_C14_Caspase3-7 | 363 | 367 | PF00656 | 0.492 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.521 |
CLV_PCSK_FUR_1 | 6 | 10 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.715 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.428 |
DEG_APCC_DBOX_1 | 158 | 166 | PF00400 | 0.506 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.726 |
DOC_CKS1_1 | 386 | 391 | PF01111 | 0.541 |
DOC_MAPK_gen_1 | 3 | 12 | PF00069 | 0.740 |
DOC_MAPK_gen_1 | 310 | 321 | PF00069 | 0.591 |
DOC_MAPK_gen_1 | 379 | 387 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 257 | 265 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 6 | 14 | PF00069 | 0.750 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.381 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.561 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.369 |
DOC_PP4_MxPP_1 | 336 | 339 | PF00568 | 0.591 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.740 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.531 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 171 | 175 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 198 | 207 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 403 | 408 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.633 |
LIG_Actin_WH2_2 | 17 | 32 | PF00022 | 0.681 |
LIG_Actin_WH2_2 | 364 | 381 | PF00022 | 0.563 |
LIG_BRCT_BRCA1_1 | 114 | 118 | PF00533 | 0.462 |
LIG_CaM_IQ_9 | 365 | 381 | PF13499 | 0.591 |
LIG_Clathr_ClatBox_1 | 318 | 322 | PF01394 | 0.561 |
LIG_deltaCOP1_diTrp_1 | 95 | 101 | PF00928 | 0.417 |
LIG_EVH1_1 | 207 | 211 | PF00568 | 0.508 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.722 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.561 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.476 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.621 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.648 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.357 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.654 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.538 |
LIG_LIR_Apic_2 | 115 | 121 | PF02991 | 0.368 |
LIG_LIR_Apic_2 | 274 | 279 | PF02991 | 0.537 |
LIG_LIR_Apic_2 | 384 | 389 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 388 | 398 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.512 |
LIG_LYPXL_S_1 | 259 | 263 | PF13949 | 0.224 |
LIG_LYPXL_yS_3 | 260 | 263 | PF13949 | 0.424 |
LIG_MLH1_MIPbox_1 | 114 | 118 | PF16413 | 0.462 |
LIG_Pex14_1 | 267 | 271 | PF04695 | 0.508 |
LIG_Pex14_2 | 64 | 68 | PF04695 | 0.369 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.379 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.508 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.490 |
LIG_SH2_NCK_1 | 285 | 289 | PF00017 | 0.561 |
LIG_SH2_PTP2 | 386 | 389 | PF00017 | 0.575 |
LIG_SH2_PTP2 | 81 | 84 | PF00017 | 0.576 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.490 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.585 |
LIG_SH3_1 | 80 | 86 | PF00018 | 0.487 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.412 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.721 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.489 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.673 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.602 |
LIG_TRAF2_1 | 419 | 422 | PF00917 | 0.782 |
MOD_CDK_SPxxK_3 | 218 | 225 | PF00069 | 0.490 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.505 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.539 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.560 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.701 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.626 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.508 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.625 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.652 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.515 |
MOD_Cter_Amidation | 281 | 284 | PF01082 | 0.331 |
MOD_DYRK1A_RPxSP_1 | 171 | 175 | PF00069 | 0.453 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.629 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.603 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.399 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.668 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.396 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.460 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.538 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.534 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.305 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.508 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.712 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.662 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.392 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.570 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.701 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.558 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.561 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.556 |
MOD_PK_1 | 33 | 39 | PF00069 | 0.746 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.408 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.504 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.485 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.673 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.678 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.599 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.746 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.520 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.472 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.518 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.509 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.482 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.561 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.562 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.714 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.477 |
TRG_DiLeu_BaEn_1 | 72 | 77 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.687 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.720 |
TRG_NLS_MonoExtC_3 | 29 | 34 | PF00514 | 0.734 |
TRG_NLS_MonoExtN_4 | 28 | 34 | PF00514 | 0.703 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.335 |
TRG_PTS2 | 1 | 14 | PF00400 | 0.697 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4U9 | Leptomonas seymouri | 68% | 100% |
A0A0S4INW4 | Bodo saltans | 40% | 100% |
A0A1X0NF48 | Trypanosomatidae | 49% | 100% |
A0A3S5H690 | Leishmania donovani | 94% | 100% |
A4H5F4 | Leishmania braziliensis | 84% | 100% |
A4HTP9 | Leishmania infantum | 94% | 100% |
C9ZPF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AMI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |