A Zn-finger protein with a TM segment on the C-terminus (2 paralogous lineages in Kinetoplastids: A4HSS9_LEIINvs. A4I356_LEIIN). Unlikely to be GPI-anchored due to reverse topology. Weakly similar to NLRC3/NOD3 intracellular immune receptor.
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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 12 |
GO:0042995 | cell projection | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005741 | mitochondrial outer membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 4 |
GO:0019867 | outer membrane | 3 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0031968 | organelle outer membrane | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H4K3
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0003729 | mRNA binding | 5 | 10 |
GO:0005488 | binding | 1 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.444 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.597 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.694 |
DEG_SPOP_SBC_1 | 300 | 304 | PF00917 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 315 | 321 | PF00134 | 0.477 |
DOC_PP1_RVXF_1 | 154 | 160 | PF00149 | 0.243 |
DOC_PP2B_LxvP_1 | 315 | 318 | PF13499 | 0.476 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.389 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.343 |
DOC_USP7_UBL2_3 | 231 | 235 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 180 | 185 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.499 |
LIG_APCC_ABBAyCdc20_2 | 19 | 25 | PF00400 | 0.440 |
LIG_EH_1 | 191 | 195 | PF12763 | 0.385 |
LIG_eIF4E_1 | 291 | 297 | PF01652 | 0.387 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.394 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.278 |
LIG_LIR_Apic_2 | 346 | 352 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 179 | 189 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.422 |
LIG_PDZ_Class_1 | 370 | 375 | PF00595 | 0.374 |
LIG_SH2_PTP2 | 267 | 270 | PF00017 | 0.261 |
LIG_SH2_SRC | 108 | 111 | PF00017 | 0.311 |
LIG_SH2_SRC | 267 | 270 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.471 |
LIG_SH3_4 | 7 | 14 | PF00018 | 0.387 |
LIG_SUMO_SIM_anti_2 | 112 | 118 | PF11976 | 0.341 |
LIG_SUMO_SIM_anti_2 | 361 | 366 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 368 | 373 | PF11976 | 0.246 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.492 |
LIG_TYR_ITIM | 106 | 111 | PF00017 | 0.363 |
LIG_WRC_WIRS_1 | 80 | 85 | PF05994 | 0.325 |
MOD_CDC14_SPxK_1 | 229 | 232 | PF00782 | 0.477 |
MOD_CDK_SPK_2 | 226 | 231 | PF00069 | 0.467 |
MOD_CDK_SPxK_1 | 226 | 232 | PF00069 | 0.470 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.356 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.352 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.628 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.645 |
MOD_Cter_Amidation | 11 | 14 | PF01082 | 0.559 |
MOD_GlcNHglycan | 133 | 137 | PF01048 | 0.371 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.593 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.603 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.575 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.706 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.561 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.526 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.391 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.514 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.522 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.419 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.413 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.368 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.415 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.717 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.575 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.480 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.295 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.455 |
MOD_PKA_1 | 18 | 24 | PF00069 | 0.596 |
MOD_PKA_1 | 200 | 206 | PF00069 | 0.569 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.471 |
MOD_PKB_1 | 308 | 316 | PF00069 | 0.627 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.361 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.460 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.649 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.792 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.457 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.419 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.334 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.475 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.706 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.624 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.559 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.495 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.531 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.263 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.366 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.560 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.705 |
MOD_SUMO_rev_2 | 203 | 212 | PF00179 | 0.505 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.443 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.563 |
TRG_NLS_MonoExtC_3 | 230 | 235 | PF00514 | 0.633 |
TRG_NLS_MonoExtN_4 | 230 | 235 | PF00514 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NM91 | Trypanosomatidae | 53% | 91% |
A0A3R7KZS1 | Trypanosoma rangeli | 53% | 92% |
A0A3S5H5P9 | Leishmania donovani | 86% | 94% |
A0A3S7X0C2 | Leishmania donovani | 21% | 100% |
A4HSS9 | Leishmania infantum | 86% | 94% |
A4I356 | Leishmania infantum | 21% | 100% |
C9ZTD5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 95% |
E9AKR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QJ41 | Leishmania major | 86% | 100% |
V5BXP3 | Trypanosoma cruzi | 58% | 92% |