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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AIA3
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0003839 | gamma-glutamylcyclotransferase activity | 5 | 7 |
GO:0016829 | lyase activity | 2 | 7 |
GO:0016840 | carbon-nitrogen lyase activity | 3 | 7 |
GO:0016842 | amidine-lyase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.520 |
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.493 |
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.265 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.744 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 485 | 487 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.603 |
DEG_APCC_DBOX_1 | 104 | 112 | PF00400 | 0.385 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.505 |
DEG_SCF_FBW7_1 | 470 | 477 | PF00400 | 0.365 |
DOC_CYCLIN_RxL_1 | 411 | 422 | PF00134 | 0.310 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 336 | 347 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 249 | 256 | PF00069 | 0.605 |
DOC_PP1_RVXF_1 | 177 | 183 | PF00149 | 0.371 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.427 |
DOC_PP4_FxxP_1 | 173 | 176 | PF00568 | 0.390 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.545 |
DOC_USP7_UBL2_3 | 485 | 489 | PF12436 | 0.630 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 384 | 388 | PF00244 | 0.429 |
LIG_CaM_NSCaTE_8 | 225 | 232 | PF13499 | 0.444 |
LIG_CSL_BTD_1 | 147 | 150 | PF09270 | 0.442 |
LIG_CtBP_PxDLS_1 | 70 | 74 | PF00389 | 0.537 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.388 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.492 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.419 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.325 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.609 |
LIG_LIR_Gen_1 | 237 | 248 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 250 | 258 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 343 | 352 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 432 | 438 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 7 | 17 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 322 | 326 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 343 | 347 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.458 |
LIG_MYND_1 | 43 | 47 | PF01753 | 0.578 |
LIG_MYND_3 | 165 | 169 | PF01753 | 0.353 |
LIG_MYND_3 | 446 | 450 | PF01753 | 0.231 |
LIG_Pex14_1 | 313 | 317 | PF04695 | 0.350 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.412 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.460 |
LIG_SH2_GRB2like | 363 | 366 | PF00017 | 0.436 |
LIG_SH2_NCK_1 | 109 | 113 | PF00017 | 0.303 |
LIG_SH2_PTP2 | 240 | 243 | PF00017 | 0.448 |
LIG_SH2_PTP2 | 344 | 347 | PF00017 | 0.344 |
LIG_SH2_SRC | 17 | 20 | PF00017 | 0.413 |
LIG_SH2_SRC | 251 | 254 | PF00017 | 0.562 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.294 |
LIG_SH2_STAP1 | 288 | 292 | PF00017 | 0.588 |
LIG_SH2_STAT3 | 436 | 439 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.692 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.207 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.522 |
LIG_SUMO_SIM_par_1 | 367 | 373 | PF11976 | 0.408 |
LIG_TRAF2_1 | 441 | 444 | PF00917 | 0.285 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.442 |
LIG_WW_1 | 93 | 96 | PF00397 | 0.518 |
MOD_CDC14_SPxK_1 | 86 | 89 | PF00782 | 0.697 |
MOD_CDK_SPK_2 | 477 | 482 | PF00069 | 0.584 |
MOD_CDK_SPxK_1 | 83 | 89 | PF00069 | 0.684 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.619 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.697 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.683 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.592 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.476 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.444 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.506 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.427 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.296 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.614 |
MOD_DYRK1A_RPxSP_1 | 89 | 93 | PF00069 | 0.536 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.621 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.455 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.551 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.698 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.551 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.510 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.797 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.448 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.787 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.513 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.377 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.680 |
MOD_N-GLC_1 | 319 | 324 | PF02516 | 0.329 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.471 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.514 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.516 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.554 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.388 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.400 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.553 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.352 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.482 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.503 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.454 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.392 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.432 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.440 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.517 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.433 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.395 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.435 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.543 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.753 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.668 |
MOD_SUMO_rev_2 | 164 | 173 | PF00179 | 0.416 |
MOD_SUMO_rev_2 | 306 | 312 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 367 | 377 | PF00179 | 0.389 |
MOD_SUMO_rev_2 | 90 | 99 | PF00179 | 0.651 |
TRG_DiLeu_BaEn_2 | 168 | 174 | PF01217 | 0.384 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 163 | 168 | PF01217 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 47 | 52 | PF01217 | 0.364 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.627 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.618 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 454 | 459 | PF00026 | 0.231 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.387 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P468 | Leptomonas seymouri | 54% | 96% |
A0A3Q8IAR7 | Leishmania donovani | 73% | 100% |
A4HYM3 | Leishmania infantum | 73% | 100% |
E9AUI8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QCZ6 | Leishmania major | 74% | 99% |