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:0005737 | cytoplasm | 2 | 9 |
GO:0005814 | centriole | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043228 | non-membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005813 | centrosome | 3 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IKC6
Term | Name | Level | Count |
---|---|---|---|
GO:0007049 | cell cycle | 2 | 9 |
GO:0009987 | cellular process | 1 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.643 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.542 |
CLV_PCSK_FUR_1 | 117 | 121 | PF00082 | 0.576 |
CLV_PCSK_FUR_1 | 150 | 154 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.542 |
CLV_PCSK_PC7_1 | 116 | 122 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.696 |
DOC_MAPK_MEF2A_6 | 26 | 35 | PF00069 | 0.499 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.697 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.672 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.626 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.657 |
LIG_14-3-3_CanoR_1 | 104 | 110 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 238 | 243 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 291 | 300 | PF00244 | 0.777 |
LIG_BIR_III_4 | 267 | 271 | PF00653 | 0.691 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.730 |
LIG_eIF4E_1 | 139 | 145 | PF01652 | 0.441 |
LIG_EVH1_2 | 322 | 326 | PF00568 | 0.770 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.539 |
LIG_LIR_Apic_2 | 271 | 275 | PF02991 | 0.694 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.595 |
LIG_SH2_STAT3 | 176 | 179 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.503 |
LIG_SH3_2 | 322 | 327 | PF14604 | 0.763 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.712 |
LIG_SUMO_SIM_anti_2 | 29 | 37 | PF11976 | 0.540 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.538 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.638 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.714 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.753 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.744 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.741 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.553 |
MOD_DYRK1A_RPxSP_1 | 240 | 244 | PF00069 | 0.696 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.707 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.738 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.690 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.459 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.631 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.599 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.715 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.679 |
MOD_LATS_1 | 236 | 242 | PF00433 | 0.688 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.536 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.752 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.744 |
MOD_NEK2_2 | 268 | 273 | PF00069 | 0.576 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.537 |
MOD_PK_1 | 238 | 244 | PF00069 | 0.719 |
MOD_PKA_1 | 40 | 46 | PF00069 | 0.537 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.623 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.679 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.566 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.622 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.706 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.603 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.577 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.610 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.665 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.664 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.656 |
MOD_SUMO_for_1 | 4 | 7 | PF00179 | 0.659 |
MOD_SUMO_for_1 | 50 | 53 | PF00179 | 0.635 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.574 |
TRG_NES_CRM1_1 | 92 | 103 | PF08389 | 0.523 |
TRG_NLS_Bipartite_1 | 63 | 85 | PF00514 | 0.570 |
TRG_NLS_MonoExtN_4 | 78 | 85 | PF00514 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.621 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2V9 | Leptomonas seymouri | 51% | 99% |
A4HPD7 | Leishmania braziliensis | 81% | 100% |
A4ICH6 | Leishmania infantum | 100% | 100% |
D0A3J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 93% |
E9AT47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q1F1 | Leishmania major | 95% | 100% |
V5BK99 | Trypanosoma cruzi | 27% | 90% |