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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AH42
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.545 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.775 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.630 |
DEG_APCC_DBOX_1 | 244 | 252 | PF00400 | 0.413 |
DEG_SPOP_SBC_1 | 216 | 220 | PF00917 | 0.639 |
DOC_CYCLIN_RxL_1 | 234 | 242 | PF00134 | 0.455 |
DOC_CYCLIN_yCln2_LP_2 | 34 | 40 | PF00134 | 0.595 |
DOC_MAPK_gen_1 | 243 | 251 | PF00069 | 0.438 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.570 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.689 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.584 |
LIG_14-3-3_CanoR_1 | 155 | 163 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 236 | 242 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 84 | 89 | PF00244 | 0.658 |
LIG_CtBP_PxDLS_1 | 255 | 259 | PF00389 | 0.515 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.511 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.543 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.606 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.731 |
LIG_LIR_Apic_2 | 117 | 123 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 203 | 213 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.392 |
LIG_NRBOX | 260 | 266 | PF00104 | 0.459 |
LIG_Pex14_2 | 21 | 25 | PF04695 | 0.667 |
LIG_Pex14_2 | 301 | 305 | PF04695 | 0.369 |
LIG_SH2_PTP2 | 205 | 208 | PF00017 | 0.390 |
LIG_SH2_PTP2 | 4 | 7 | PF00017 | 0.677 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 180 | 183 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.681 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.658 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.631 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.588 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.532 |
LIG_SUMO_SIM_par_1 | 237 | 242 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 246 | 253 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 254 | 260 | PF11976 | 0.416 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.405 |
MOD_CDK_SPK_2 | 217 | 222 | PF00069 | 0.629 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.633 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.557 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.437 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.586 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.683 |
MOD_Cter_Amidation | 16 | 19 | PF01082 | 0.622 |
MOD_DYRK1A_RPxSP_1 | 91 | 95 | PF00069 | 0.689 |
MOD_GlcNHglycan | 144 | 148 | PF01048 | 0.630 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.660 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.573 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.531 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.648 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.619 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.507 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.498 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.725 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.494 |
MOD_LATS_1 | 68 | 74 | PF00433 | 0.710 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.648 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.603 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.616 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.714 |
MOD_PKA_1 | 84 | 90 | PF00069 | 0.624 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.637 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.617 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.644 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.604 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.657 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.724 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.587 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.592 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.595 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.635 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.585 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.561 |
TRG_NES_CRM1_1 | 246 | 260 | PF08389 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 237 | 242 | PF00026 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1G9 | Leptomonas seymouri | 63% | 100% |
A0A1X0NJB4 | Trypanosomatidae | 37% | 100% |
A0A3Q8IB82 | Leishmania donovani | 100% | 100% |
A0A3R7RTA5 | Trypanosoma rangeli | 37% | 100% |
A4HD87 | Leishmania braziliensis | 82% | 100% |
D0A6Z9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AWM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QAV0 | Leishmania major | 92% | 100% |
V5C0R1 | Trypanosoma cruzi | 39% | 100% |