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: Q4Q110
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 106 | 112 | PF00089 | 0.269 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.233 |
CLV_PCSK_FUR_1 | 253 | 257 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 255 | 257 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 285 | 287 | PF00082 | 0.750 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.340 |
DEG_SCF_FBW7_1 | 47 | 53 | PF00400 | 0.433 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.433 |
DOC_CYCLIN_RxL_1 | 243 | 250 | PF00134 | 0.576 |
DOC_CYCLIN_RxL_1 | 325 | 335 | PF00134 | 0.474 |
DOC_MAPK_gen_1 | 295 | 302 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 212 | 220 | PF00069 | 0.550 |
DOC_PP1_RVXF_1 | 297 | 303 | PF00149 | 0.373 |
DOC_PP1_SILK_1 | 154 | 159 | PF00149 | 0.433 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.533 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 203 | 209 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 286 | 296 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 358 | 362 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 366 | 372 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 386 | 392 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 65 | 69 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 92 | 97 | PF00244 | 0.540 |
LIG_Actin_WH2_2 | 21 | 38 | PF00022 | 0.531 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.787 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.510 |
LIG_BRCT_BRCA1_1 | 347 | 351 | PF00533 | 0.564 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.495 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.552 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.480 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.531 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.707 |
LIG_LIR_Gen_1 | 79 | 90 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.479 |
LIG_PTB_Apo_2 | 391 | 398 | PF02174 | 0.575 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.506 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.531 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 420 | 424 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.508 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.574 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.566 |
LIG_TYR_ITIM | 23 | 28 | PF00017 | 0.424 |
LIG_UBA3_1 | 248 | 255 | PF00899 | 0.602 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.537 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.552 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.675 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.564 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.507 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.647 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.508 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.569 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.676 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.610 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.579 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.617 |
MOD_Cter_Amidation | 57 | 60 | PF01082 | 0.233 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.299 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.281 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.371 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.316 |
MOD_GlcNHglycan | 261 | 265 | PF01048 | 0.692 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.794 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.679 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.731 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.329 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.278 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.497 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.690 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.739 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.285 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.459 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.448 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.340 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.531 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.650 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.635 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.252 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.495 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.479 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.715 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.469 |
MOD_PK_1 | 204 | 210 | PF00069 | 0.476 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.587 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.696 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.778 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.564 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.546 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.433 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.548 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.502 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.551 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.240 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.576 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.573 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.483 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.692 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.495 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.477 |
TRG_DiLeu_BaEn_3 | 10 | 16 | PF01217 | 0.549 |
TRG_DiLeu_BaEn_4 | 11 | 17 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.576 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.675 |
TRG_ER_diArg_1 | 202 | 204 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.551 |
TRG_NLS_MonoCore_2 | 251 | 256 | PF00514 | 0.516 |
TRG_NLS_MonoExtC_3 | 251 | 256 | PF00514 | 0.579 |
TRG_NLS_MonoExtN_4 | 252 | 259 | PF00514 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 219 | 223 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEL6 | Leptomonas seymouri | 50% | 100% |
A0A0S4JGI4 | Bodo saltans | 36% | 100% |
A0A1X0P3J3 | Trypanosomatidae | 35% | 100% |
A0A3S5IS07 | Trypanosoma rangeli | 41% | 100% |
A0A3S7XBG3 | Leishmania donovani | 88% | 100% |
A4ICZ0 | Leishmania infantum | 88% | 100% |
D0A8N8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9ATI8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |