Unique Kinetoplastid protein of unclear topology and structure. Might not be a TM protein.
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4HED2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.581 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.469 |
CLV_PCSK_FUR_1 | 199 | 203 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.219 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.219 |
CLV_PCSK_PC1ET2_1 | 401 | 403 | PF00082 | 0.626 |
CLV_PCSK_PC7_1 | 198 | 204 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.367 |
CLV_Separin_Metazoa | 151 | 155 | PF03568 | 0.658 |
DEG_SPOP_SBC_1 | 124 | 128 | PF00917 | 0.577 |
DOC_CDC14_PxL_1 | 57 | 65 | PF14671 | 0.647 |
DOC_CYCLIN_RxL_1 | 9 | 22 | PF00134 | 0.604 |
DOC_CYCLIN_yClb1_LxF_4 | 13 | 18 | PF00134 | 0.609 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 231 | PF00134 | 0.363 |
DOC_CYCLIN_yCln2_LP_2 | 301 | 307 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 404 | 410 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 164 | 174 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 167 | 176 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 310 | 319 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 69 | 76 | PF00069 | 0.608 |
DOC_PP1_RVXF_1 | 12 | 19 | PF00149 | 0.603 |
DOC_PP1_RVXF_1 | 165 | 171 | PF00149 | 0.556 |
DOC_PP1_RVXF_1 | 270 | 276 | PF00149 | 0.284 |
DOC_PP1_RVXF_1 | 430 | 436 | PF00149 | 0.426 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.334 |
DOC_PP2B_LxvP_1 | 404 | 407 | PF13499 | 0.420 |
DOC_PP2B_LxvP_1 | 63 | 66 | PF13499 | 0.607 |
DOC_PP4_FxxP_1 | 449 | 452 | PF00568 | 0.265 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.481 |
DOC_USP7_UBL2_3 | 422 | 426 | PF12436 | 0.431 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 328 | 337 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 9 | 13 | PF00244 | 0.614 |
LIG_Actin_WH2_2 | 347 | 362 | PF00022 | 0.414 |
LIG_AP2alpha_1 | 445 | 449 | PF02296 | 0.442 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.702 |
LIG_BIR_III_4 | 238 | 242 | PF00653 | 0.452 |
LIG_BRCT_BRCA1_1 | 310 | 314 | PF00533 | 0.472 |
LIG_EH1_1 | 256 | 264 | PF00400 | 0.245 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.549 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.415 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.292 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.378 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.452 |
LIG_LIR_Apic_2 | 447 | 452 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 443 | 448 | PF02991 | 0.361 |
LIG_MYND_1 | 335 | 339 | PF01753 | 0.422 |
LIG_NRBOX | 167 | 173 | PF00104 | 0.493 |
LIG_PCNA_yPIPBox_3 | 129 | 143 | PF02747 | 0.623 |
LIG_Pex14_1 | 192 | 196 | PF04695 | 0.355 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.394 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.441 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.358 |
LIG_SH2_NCK_1 | 236 | 240 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.164 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.596 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.587 |
LIG_SUMO_SIM_anti_2 | 258 | 263 | PF11976 | 0.258 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.563 |
LIG_TYR_ITIM | 179 | 184 | PF00017 | 0.424 |
LIG_WW_1 | 222 | 225 | PF00397 | 0.366 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.674 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.532 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.401 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.412 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.457 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.376 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.594 |
MOD_Cter_Amidation | 37 | 40 | PF01082 | 0.307 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.483 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.710 |
MOD_GlcNHglycan | 367 | 371 | PF01048 | 0.577 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.683 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.360 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.735 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.397 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.444 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.496 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.410 |
MOD_NEK2_2 | 162 | 167 | PF00069 | 0.485 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.604 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.720 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.552 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.477 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.613 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.301 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.594 |
MOD_Plk_2-3 | 291 | 297 | PF00069 | 0.418 |
MOD_Plk_2-3 | 447 | 453 | PF00069 | 0.457 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.563 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.618 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.418 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.388 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.400 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.309 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.580 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 72 | 77 | PF01217 | 0.676 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.244 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.601 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.656 |
TRG_NES_CRM1_1 | 439 | 453 | PF08389 | 0.421 |
TRG_NLS_MonoExtC_3 | 13 | 19 | PF00514 | 0.620 |
TRG_NLS_MonoExtN_4 | 13 | 18 | PF00514 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 100 | 104 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYH4 | Leptomonas seymouri | 64% | 97% |
A0A0S4J1E4 | Bodo saltans | 40% | 100% |
A0A1X0NYG5 | Trypanosomatidae | 49% | 100% |
A0A3Q8ICN7 | Leishmania donovani | 85% | 100% |
C9ZKD5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AXW1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q95ZC0 | Leishmania major | 85% | 100% |
V5BH15 | Trypanosoma cruzi | 48% | 100% |