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 |
Related structures:
AlphaFold database: Q4QEB6
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 1 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.769 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.806 |
CLV_PCSK_FUR_1 | 436 | 440 | PF00082 | 0.811 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.776 |
CLV_PCSK_PC1ET2_1 | 137 | 139 | PF00082 | 0.369 |
CLV_PCSK_PC7_1 | 133 | 139 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.620 |
CLV_Separin_Metazoa | 433 | 437 | PF03568 | 0.680 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.467 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.685 |
DEG_SPOP_SBC_1 | 422 | 426 | PF00917 | 0.588 |
DEG_SPOP_SBC_1 | 73 | 77 | PF00917 | 0.468 |
DOC_ANK_TNKS_1 | 440 | 447 | PF00023 | 0.768 |
DOC_CKS1_1 | 247 | 252 | PF01111 | 0.584 |
DOC_CYCLIN_yCln2_LP_2 | 247 | 253 | PF00134 | 0.575 |
DOC_CYCLIN_yCln2_LP_2 | 83 | 89 | PF00134 | 0.408 |
DOC_PP1_RVXF_1 | 394 | 400 | PF00149 | 0.426 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.502 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.408 |
DOC_PP4_FxxP_1 | 429 | 432 | PF00568 | 0.718 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.790 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.462 |
DOC_USP7_UBL2_3 | 166 | 170 | PF12436 | 0.478 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 115 | 125 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 396 | 405 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 421 | 431 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.487 |
LIG_BRCT_BRCA1_1 | 193 | 197 | PF00533 | 0.689 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.792 |
LIG_eIF4E_1 | 272 | 278 | PF01652 | 0.481 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.627 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.648 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.557 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.459 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.397 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.383 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.411 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.524 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.767 |
LIG_LIR_Apic_2 | 18 | 24 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 258 | 264 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 426 | 432 | PF02991 | 0.714 |
LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 299 | 308 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 325 | 335 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 362 | 371 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.369 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.482 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.452 |
LIG_SH2_PTP2 | 253 | 256 | PF00017 | 0.467 |
LIG_SH2_PTP2 | 363 | 366 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.447 |
LIG_SH3_2 | 432 | 437 | PF14604 | 0.717 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.810 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.411 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.299 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.408 |
LIG_TYR_ITIM | 361 | 366 | PF00017 | 0.484 |
LIG_WW_3 | 433 | 437 | PF00397 | 0.719 |
MOD_CDK_SPK_2 | 183 | 188 | PF00069 | 0.660 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.468 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.689 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.575 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.474 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.445 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.369 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.573 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.502 |
MOD_Cter_Amidation | 310 | 313 | PF01082 | 0.385 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.507 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.622 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.706 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.688 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.612 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.408 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.428 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.242 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.589 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.482 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.654 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.664 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.558 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.489 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.656 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.453 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.645 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.613 |
MOD_N-GLC_2 | 289 | 291 | PF02516 | 0.387 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.548 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.384 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.383 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.388 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.606 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.633 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.155 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.344 |
MOD_PKA_1 | 437 | 443 | PF00069 | 0.736 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.320 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.492 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.406 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.426 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.708 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.783 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.602 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.573 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.506 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.552 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.699 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.583 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.469 |
MOD_SUMO_for_1 | 222 | 225 | PF00179 | 0.477 |
MOD_SUMO_for_1 | 405 | 408 | PF00179 | 0.616 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 396 | 399 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.802 |
TRG_NES_CRM1_1 | 123 | 136 | PF08389 | 0.444 |
TRG_NES_CRM1_1 | 167 | 179 | PF08389 | 0.531 |
TRG_NLS_MonoCore_2 | 468 | 473 | PF00514 | 0.615 |
TRG_NLS_MonoExtC_3 | 469 | 474 | PF00514 | 0.773 |
TRG_NLS_MonoExtN_4 | 469 | 475 | PF00514 | 0.811 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWR5 | Leptomonas seymouri | 59% | 100% |
A0A1X0NSU1 | Trypanosomatidae | 41% | 100% |
A0A3S7WUF8 | Leishmania donovani | 93% | 100% |
A0A422N4P6 | Trypanosoma rangeli | 41% | 100% |
A4H920 | Leishmania braziliensis | 77% | 100% |
A4HXF2 | Leishmania infantum | 93% | 100% |
C9ZP24 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AR47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |