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: E9AR47
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_NRD_NRD_1 | 368 | 370 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.783 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.593 |
CLV_PCSK_FUR_1 | 436 | 440 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 137 | 139 | PF00082 | 0.288 |
CLV_PCSK_PC1ET2_1 | 471 | 473 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 133 | 139 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.596 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.383 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.671 |
DEG_SPOP_SBC_1 | 422 | 426 | PF00917 | 0.665 |
DEG_SPOP_SBC_1 | 74 | 78 | PF00917 | 0.375 |
DOC_CKS1_1 | 247 | 252 | PF01111 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 247 | 253 | PF00134 | 0.455 |
DOC_CYCLIN_yCln2_LP_2 | 83 | 89 | PF00134 | 0.312 |
DOC_PP1_RVXF_1 | 394 | 400 | PF00149 | 0.408 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.384 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.312 |
DOC_PP4_FxxP_1 | 429 | 432 | PF00568 | 0.630 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.313 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.275 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.179 |
DOC_USP7_UBL2_3 | 166 | 170 | PF12436 | 0.415 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.405 |
LIG_14-3-3_CanoR_1 | 115 | 125 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 337 | 347 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 396 | 405 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.366 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.673 |
LIG_eIF4E_1 | 272 | 278 | PF01652 | 0.435 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.552 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.496 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.399 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.414 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.384 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.321 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.349 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.443 |
LIG_LIR_Apic_2 | 18 | 24 | PF02991 | 0.458 |
LIG_LIR_Apic_2 | 258 | 264 | PF02991 | 0.382 |
LIG_LIR_Apic_2 | 426 | 432 | PF02991 | 0.626 |
LIG_LIR_Apic_2 | 68 | 74 | PF02991 | 0.231 |
LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 299 | 308 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 325 | 335 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 362 | 371 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.348 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.382 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.432 |
LIG_SH2_PTP2 | 253 | 256 | PF00017 | 0.423 |
LIG_SH2_PTP2 | 363 | 366 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.193 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.394 |
LIG_SH3_2 | 432 | 437 | PF14604 | 0.626 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.375 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.812 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.351 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.312 |
LIG_TRFH_1 | 71 | 75 | PF08558 | 0.300 |
LIG_TYR_ITIM | 361 | 366 | PF00017 | 0.440 |
LIG_UBA3_1 | 1 | 7 | PF00899 | 0.311 |
LIG_WW_3 | 433 | 437 | PF00397 | 0.626 |
MOD_CDK_SPxK_1 | 242 | 248 | PF00069 | 0.480 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.622 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.371 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.707 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.481 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.425 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.414 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.321 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.476 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.414 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.548 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.254 |
MOD_Cter_Amidation | 310 | 313 | PF01082 | 0.339 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.497 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.503 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.594 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.727 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.687 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.605 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.400 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.312 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.262 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.454 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.656 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.459 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.462 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.595 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.531 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.684 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.437 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.559 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.360 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.563 |
MOD_N-GLC_2 | 289 | 291 | PF02516 | 0.323 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.454 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.307 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.324 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.334 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.426 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.284 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.481 |
MOD_PK_1 | 441 | 447 | PF00069 | 0.508 |
MOD_PKA_1 | 437 | 443 | PF00069 | 0.643 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.347 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.785 |
MOD_PKB_1 | 439 | 447 | PF00069 | 0.508 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.457 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.404 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.508 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.438 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.459 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.427 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.179 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.652 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.404 |
MOD_SUMO_for_1 | 222 | 225 | PF00179 | 0.375 |
MOD_SUMO_for_1 | 405 | 408 | PF00179 | 0.587 |
TRG_DiLeu_LyEn_5 | 123 | 128 | PF01217 | 0.179 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 396 | 399 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.798 |
TRG_NES_CRM1_1 | 123 | 136 | PF08389 | 0.422 |
TRG_NES_CRM1_1 | 167 | 179 | PF08389 | 0.456 |
TRG_NLS_MonoCore_2 | 468 | 473 | PF00514 | 0.580 |
TRG_NLS_MonoExtC_3 | 468 | 473 | PF00514 | 0.746 |
TRG_NLS_MonoExtN_4 | 469 | 475 | PF00514 | 0.698 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWR5 | Leptomonas seymouri | 58% | 100% |
A0A1X0NSU1 | Trypanosomatidae | 39% | 100% |
A0A3S7WUF8 | Leishmania donovani | 91% | 100% |
A0A422N4P6 | Trypanosoma rangeli | 40% | 100% |
A4H920 | Leishmania braziliensis | 77% | 98% |
A4HXF2 | Leishmania infantum | 91% | 100% |
C9ZP24 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
Q4QEB6 | Leishmania major | 90% | 100% |