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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9AUN2
Term | Name | Level | Count |
---|---|---|---|
GO:0000413 | protein peptidyl-prolyl isomerization | 7 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0018193 | peptidyl-amino acid modification | 5 | 12 |
GO:0018208 | peptidyl-proline modification | 6 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016859 | cis-trans isomerase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.695 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.473 |
CLV_PCSK_FUR_1 | 254 | 258 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 318 | 320 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.784 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.409 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.385 |
DEG_SPOP_SBC_1 | 395 | 399 | PF00917 | 0.744 |
DOC_CKS1_1 | 157 | 162 | PF01111 | 0.599 |
DOC_CKS1_1 | 62 | 67 | PF01111 | 0.533 |
DOC_CYCLIN_yCln2_LP_2 | 43 | 49 | PF00134 | 0.539 |
DOC_MAPK_FxFP_2 | 7 | 10 | PF00069 | 0.366 |
DOC_MAPK_gen_1 | 299 | 308 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 83 | 92 | PF00069 | 0.402 |
DOC_MAPK_HePTP_8 | 296 | 308 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 299 | 308 | PF00069 | 0.431 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.573 |
DOC_PP2B_LxvP_1 | 43 | 46 | PF13499 | 0.530 |
DOC_PP4_FxxP_1 | 20 | 23 | PF00568 | 0.411 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.366 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.694 |
DOC_USP7_MATH_2 | 46 | 52 | PF00917 | 0.464 |
DOC_USP7_UBL2_3 | 427 | 431 | PF12436 | 0.770 |
DOC_USP7_UBL2_3 | 432 | 436 | PF12436 | 0.678 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 109 | 113 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 184 | 193 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 28 | 33 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 336 | 342 | PF00244 | 0.704 |
LIG_Actin_WH2_2 | 168 | 185 | PF00022 | 0.556 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.673 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.634 |
LIG_BRCT_BRCA1_1 | 421 | 425 | PF00533 | 0.590 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.469 |
LIG_BRCT_BRCA1_2 | 289 | 295 | PF00533 | 0.700 |
LIG_BRCT_BRCA1_2 | 296 | 302 | PF00533 | 0.651 |
LIG_BRCT_BRCA1_2 | 421 | 427 | PF00533 | 0.589 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.469 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.629 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.388 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.574 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.602 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.529 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.473 |
LIG_LIR_Apic_2 | 19 | 23 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 4 | 10 | PF02991 | 0.364 |
LIG_LIR_Apic_2 | 59 | 65 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 165 | 172 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.398 |
LIG_MLH1_MIPbox_1 | 290 | 294 | PF16413 | 0.679 |
LIG_PTB_Apo_2 | 31 | 38 | PF02174 | 0.351 |
LIG_REV1ctd_RIR_1 | 291 | 299 | PF16727 | 0.713 |
LIG_REV1ctd_RIR_1 | 355 | 363 | PF16727 | 0.638 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.539 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.532 |
LIG_SH2_PTP2 | 151 | 154 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.545 |
LIG_SH3_1 | 241 | 247 | PF00018 | 0.706 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.496 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.524 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.706 |
LIG_TYR_ITIM | 135 | 140 | PF00017 | 0.519 |
LIG_TYR_ITIM | 211 | 216 | PF00017 | 0.609 |
MOD_CDK_SPxxK_3 | 156 | 163 | PF00069 | 0.500 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.708 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.723 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.593 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.408 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.538 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.497 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.505 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.444 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.416 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.648 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.606 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.720 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.501 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.719 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.730 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.354 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.427 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.582 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.561 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.628 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.727 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.670 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.661 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.396 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.571 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.630 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.567 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.624 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.395 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.763 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.411 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.588 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.427 |
MOD_PK_1 | 119 | 125 | PF00069 | 0.596 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.558 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.774 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.616 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.532 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.473 |
MOD_Plk_2-3 | 85 | 91 | PF00069 | 0.516 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.421 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.490 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.470 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.455 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.340 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.570 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.556 |
MOD_SUMO_rev_2 | 177 | 185 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 66 | 71 | PF00179 | 0.391 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.618 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.742 |
TRG_ER_diLys_1 | 434 | 438 | PF00400 | 0.580 |
TRG_NLS_Bipartite_1 | 183 | 203 | PF00514 | 0.590 |
TRG_NLS_MonoCore_2 | 317 | 322 | PF00514 | 0.672 |
TRG_NLS_MonoExtC_3 | 317 | 323 | PF00514 | 0.611 |
TRG_NLS_MonoExtC_3 | 430 | 435 | PF00514 | 0.743 |
TRG_NLS_MonoExtN_4 | 198 | 203 | PF00514 | 0.577 |
TRG_NLS_MonoExtN_4 | 315 | 322 | PF00514 | 0.645 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC45 | Leptomonas seymouri | 58% | 100% |
A0A0S4KRJ3 | Bodo saltans | 32% | 100% |
A0A1X0NWC9 | Trypanosomatidae | 33% | 100% |
A0A3S7WVY2 | Leishmania donovani | 86% | 100% |
A0A422NPI7 | Trypanosoma rangeli | 36% | 100% |
A4HYT6 | Leishmania infantum | 87% | 95% |
C9ZIB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AIE5 | Leishmania braziliensis | 72% | 98% |
Q4QCV2 | Leishmania major | 87% | 100% |
V5DRZ7 | Trypanosoma cruzi | 37% | 100% |