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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 2 |
GO:0005689 | U12-type spliceosomal complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q715
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.666 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.666 |
DEG_SPOP_SBC_1 | 142 | 146 | PF00917 | 0.645 |
DEG_SPOP_SBC_1 | 279 | 283 | PF00917 | 0.517 |
DOC_PP1_RVXF_1 | 226 | 233 | PF00149 | 0.624 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.446 |
DOC_USP7_MATH_2 | 141 | 147 | PF00917 | 0.566 |
DOC_USP7_UBL2_3 | 297 | 301 | PF12436 | 0.241 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 15 | 24 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 191 | 199 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 227 | 231 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 308 | 312 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 70 | 74 | PF00244 | 0.394 |
LIG_APCC_ABBA_1 | 210 | 215 | PF00400 | 0.633 |
LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.658 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.598 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.569 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.739 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.543 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.610 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.597 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.712 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.360 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.528 |
LIG_KLC1_Yacidic_2 | 211 | 215 | PF13176 | 0.589 |
LIG_LIR_Apic_2 | 93 | 99 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.465 |
LIG_SH2_SRC | 27 | 30 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.485 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.682 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.584 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.545 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.564 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.626 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.641 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.613 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.661 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.581 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.609 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.415 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.711 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.465 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.561 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.315 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.488 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.599 |
MOD_Cter_Amidation | 171 | 174 | PF01082 | 0.632 |
MOD_DYRK1A_RPxSP_1 | 256 | 260 | PF00069 | 0.622 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.660 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.619 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.463 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.483 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.334 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.578 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.730 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.637 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.746 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.309 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.489 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.567 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.631 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.566 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.448 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.326 |
MOD_PKA_1 | 173 | 179 | PF00069 | 0.615 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.487 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.621 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.634 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.381 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.401 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.564 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.620 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.592 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.598 |
MOD_SUMO_rev_2 | 146 | 155 | PF00179 | 0.648 |
MOD_SUMO_rev_2 | 170 | 179 | PF00179 | 0.620 |
TRG_DiLeu_BaEn_1 | 42 | 47 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_2 | 285 | 291 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 159 | 164 | PF01217 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 138 | 143 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD74 | Leptomonas seymouri | 32% | 99% |
A0A3S7X3N7 | Leishmania donovani | 90% | 100% |
A4HIL1 | Leishmania braziliensis | 67% | 72% |
A4I5V6 | Leishmania infantum | 90% | 100% |
E9B151 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |