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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H3W9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 119 | 123 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.753 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.638 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.607 |
CLV_PCSK_PC7_1 | 193 | 199 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.594 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.613 |
DEG_SPOP_SBC_1 | 231 | 235 | PF00917 | 0.627 |
DOC_CYCLIN_RxL_1 | 28 | 39 | PF00134 | 0.514 |
DOC_MAPK_gen_1 | 34 | 40 | PF00069 | 0.444 |
DOC_PP2B_LxvP_1 | 95 | 98 | PF13499 | 0.506 |
DOC_PP4_FxxP_1 | 208 | 211 | PF00568 | 0.490 |
DOC_PP4_FxxP_1 | 58 | 61 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.598 |
DOC_USP7_UBL2_3 | 199 | 203 | PF12436 | 0.653 |
DOC_USP7_UBL2_3 | 309 | 313 | PF12436 | 0.578 |
DOC_USP7_UBL2_3 | 318 | 322 | PF12436 | 0.646 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.576 |
LIG_Actin_WH2_2 | 78 | 96 | PF00022 | 0.592 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.468 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.568 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.542 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.504 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.702 |
LIG_LIR_Apic_2 | 207 | 211 | PF02991 | 0.493 |
LIG_LIR_Apic_2 | 88 | 92 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 115 | 126 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.556 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.591 |
LIG_SH2_NCK_1 | 118 | 122 | PF00017 | 0.585 |
LIG_SH2_SRC | 182 | 185 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.726 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.569 |
LIG_SH3_2 | 49 | 54 | PF14604 | 0.591 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.549 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.539 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.630 |
LIG_TRAF2_1 | 48 | 51 | PF00917 | 0.577 |
LIG_TYR_ITIM | 116 | 121 | PF00017 | 0.595 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.517 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.512 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.674 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.672 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.658 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.618 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.573 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.454 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.579 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.638 |
MOD_Cter_Amidation | 195 | 198 | PF01082 | 0.519 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.666 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.769 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.748 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.550 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.558 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.549 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.487 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.753 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.671 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.561 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.533 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.610 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.622 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.467 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.598 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.540 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.470 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.671 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.524 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.530 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.491 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.715 |
MOD_PKB_1 | 28 | 36 | PF00069 | 0.345 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.496 |
MOD_Plk_2-3 | 249 | 255 | PF00069 | 0.526 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.543 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.593 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.698 |
TRG_NLS_Bipartite_1 | 10 | 31 | PF00514 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II41 | Leptomonas seymouri | 60% | 100% |
A0A1X0NL53 | Trypanosomatidae | 38% | 100% |
A0A3S7WNR7 | Leishmania donovani | 80% | 100% |
A4HS44 | Leishmania infantum | 79% | 100% |
E9AK31 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
O97206 | Leishmania major | 77% | 98% |
V5B9E1 | Trypanosoma cruzi | 38% | 100% |