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 | yes | yes: 1, no: 12 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 14 |
GO:0042995 | cell projection | 2 | 14 |
GO:0043226 | organelle | 2 | 14 |
GO:0043227 | membrane-bounded organelle | 3 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 14 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005741 | mitochondrial outer membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 6 |
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: A4HSS9
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 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043169 | cation binding | 3 | 14 |
GO:0046872 | metal ion binding | 4 | 14 |
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 | 102 | 106 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.617 |
CLV_PCSK_FUR_1 | 38 | 42 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.752 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.658 |
CLV_PCSK_PC1ET2_1 | 257 | 259 | PF00082 | 0.733 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.703 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 341 | 347 | PF00134 | 0.452 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.461 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.239 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.543 |
DOC_USP7_UBL2_3 | 257 | 261 | PF12436 | 0.495 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.510 |
LIG_APCC_ABBA_1 | 107 | 112 | PF00400 | 0.397 |
LIG_APCC_ABBAyCdc20_2 | 46 | 52 | PF00400 | 0.424 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.468 |
LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.513 |
LIG_EH_1 | 218 | 222 | PF12763 | 0.392 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.478 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.402 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.438 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.606 |
LIG_LIR_Gen_1 | 105 | 115 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 206 | 216 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.460 |
LIG_NRBOX | 9 | 15 | PF00104 | 0.417 |
LIG_SH2_NCK_1 | 311 | 315 | PF00017 | 0.422 |
LIG_SH2_PTP2 | 293 | 296 | PF00017 | 0.263 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.309 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.276 |
LIG_SH2_SRC | 361 | 364 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.437 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 139 | 145 | PF11976 | 0.342 |
LIG_SUMO_SIM_anti_2 | 387 | 392 | PF11976 | 0.377 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.496 |
LIG_TRFH_1 | 12 | 16 | PF08558 | 0.456 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.358 |
LIG_UBA3_1 | 143 | 148 | PF00899 | 0.350 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.337 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.352 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.615 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.604 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.738 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.629 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.467 |
MOD_GlcNHglycan | 160 | 164 | PF01048 | 0.371 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.631 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.608 |
MOD_GlcNHglycan | 315 | 319 | PF01048 | 0.651 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.601 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.687 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.391 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.563 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.719 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.603 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.423 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.408 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.276 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.391 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.732 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.578 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.301 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.579 |
MOD_PK_1 | 197 | 203 | PF00069 | 0.395 |
MOD_PKA_1 | 227 | 233 | PF00069 | 0.604 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.572 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.503 |
MOD_PKB_1 | 334 | 342 | PF00069 | 0.616 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.420 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.414 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.455 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.454 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.667 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.754 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.720 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.362 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.352 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.746 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.465 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.472 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.631 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.532 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.546 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.264 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.685 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.605 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.765 |
MOD_SUMO_rev_2 | 230 | 238 | PF00179 | 0.550 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.721 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.543 |
TRG_NES_CRM1_1 | 3 | 18 | PF08389 | 0.411 |
TRG_NLS_MonoExtC_3 | 256 | 261 | PF00514 | 0.650 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NM91 | Trypanosomatidae | 53% | 97% |
A0A3R7KZS1 | Trypanosoma rangeli | 54% | 99% |
A0A3S5H5P9 | Leishmania donovani | 100% | 100% |
A0A3S7X0C2 | Leishmania donovani | 22% | 100% |
A4H4K3 | Leishmania braziliensis | 86% | 100% |
A4HFD8 | Leishmania braziliensis | 21% | 100% |
A4I356 | Leishmania infantum | 22% | 100% |
C9ZTD5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AKR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AYS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
Q4QJ41 | Leishmania major | 96% | 100% |
V5BXP3 | Trypanosoma cruzi | 58% | 99% |