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: Q95ZC0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.459 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.490 |
CLV_PCSK_PC7_1 | 198 | 204 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.384 |
CLV_Separin_Metazoa | 151 | 155 | PF03568 | 0.653 |
DEG_APCC_DBOX_1 | 382 | 390 | PF00400 | 0.419 |
DOC_CDC14_PxL_1 | 57 | 65 | PF14671 | 0.636 |
DOC_CYCLIN_RxL_1 | 9 | 22 | PF00134 | 0.599 |
DOC_CYCLIN_yClb1_LxF_4 | 13 | 18 | PF00134 | 0.611 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 231 | PF00134 | 0.365 |
DOC_CYCLIN_yCln2_LP_2 | 301 | 307 | PF00134 | 0.510 |
DOC_CYCLIN_yCln2_LP_2 | 404 | 410 | PF00134 | 0.422 |
DOC_MAPK_DCC_7 | 297 | 307 | PF00069 | 0.353 |
DOC_MAPK_gen_1 | 164 | 174 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 297 | 307 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 81 | 90 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 167 | 176 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 300 | 307 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 310 | 319 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 69 | 76 | PF00069 | 0.607 |
DOC_PP1_RVXF_1 | 12 | 19 | PF00149 | 0.604 |
DOC_PP1_RVXF_1 | 165 | 171 | PF00149 | 0.556 |
DOC_PP1_RVXF_1 | 374 | 380 | PF00149 | 0.425 |
DOC_PP1_RVXF_1 | 430 | 436 | PF00149 | 0.427 |
DOC_PP1_RVXF_1 | 99 | 106 | PF00149 | 0.613 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.336 |
DOC_PP2B_LxvP_1 | 404 | 407 | PF13499 | 0.423 |
DOC_PP2B_LxvP_1 | 63 | 66 | PF13499 | 0.595 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.432 |
DOC_USP7_UBL2_3 | 422 | 426 | PF12436 | 0.431 |
LIG_14-3-3_CanoR_1 | 116 | 121 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 328 | 333 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 9 | 13 | PF00244 | 0.597 |
LIG_Actin_WH2_2 | 347 | 362 | PF00022 | 0.421 |
LIG_Actin_WH2_2 | 70 | 86 | PF00022 | 0.617 |
LIG_AP2alpha_1 | 445 | 449 | PF02296 | 0.448 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.684 |
LIG_BIR_III_4 | 238 | 242 | PF00653 | 0.452 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.425 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.384 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.452 |
LIG_LIR_Gen_1 | 160 | 170 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 273 | 282 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 443 | 448 | PF02991 | 0.368 |
LIG_MYND_1 | 335 | 339 | PF01753 | 0.424 |
LIG_PCNA_PIPBox_1 | 64 | 73 | PF02747 | 0.521 |
LIG_PCNA_yPIPBox_3 | 37 | 51 | PF02747 | 0.604 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.407 |
LIG_PTB_Apo_2 | 35 | 42 | PF02174 | 0.606 |
LIG_PTB_Phospho_1 | 35 | 41 | PF10480 | 0.612 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.439 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.361 |
LIG_SH2_NCK_1 | 236 | 240 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.165 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.593 |
LIG_SH2_STAT3 | 41 | 44 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.396 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.478 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.364 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.386 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.582 |
LIG_TYR_ITIM | 179 | 184 | PF00017 | 0.402 |
LIG_TYR_ITIM | 189 | 194 | PF00017 | 0.332 |
LIG_UBA3_1 | 76 | 84 | PF00899 | 0.675 |
LIG_WW_1 | 222 | 225 | PF00397 | 0.370 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.542 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.406 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.416 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.467 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.377 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.402 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.530 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.487 |
MOD_GlcNHglycan | 367 | 371 | PF01048 | 0.584 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.606 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.369 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.561 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.740 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.451 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.515 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.410 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.626 |
MOD_NEK2_2 | 270 | 275 | PF00069 | 0.349 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.599 |
MOD_PK_1 | 116 | 122 | PF00069 | 0.563 |
MOD_PK_1 | 328 | 334 | PF00069 | 0.365 |
MOD_PKA_1 | 116 | 122 | PF00069 | 0.607 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.705 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.488 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.603 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.671 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.374 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.357 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.482 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.301 |
MOD_Plk_2-3 | 291 | 297 | PF00069 | 0.437 |
MOD_Plk_2-3 | 447 | 453 | PF00069 | 0.461 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.630 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.421 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.389 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.368 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.310 |
MOD_SUMO_rev_2 | 104 | 113 | PF00179 | 0.649 |
MOD_SUMO_rev_2 | 387 | 395 | PF00179 | 0.451 |
TRG_DiLeu_BaEn_3 | 97 | 103 | PF01217 | 0.616 |
TRG_DiLeu_BaLyEn_6 | 72 | 77 | PF01217 | 0.670 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.579 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.313 |
TRG_NES_CRM1_1 | 439 | 453 | PF08389 | 0.425 |
TRG_NLS_MonoExtC_3 | 13 | 19 | PF00514 | 0.620 |
TRG_NLS_MonoExtN_4 | 13 | 18 | PF00514 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 100 | 104 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYH4 | Leptomonas seymouri | 67% | 97% |
A0A0S4J1E4 | Bodo saltans | 40% | 100% |
A0A1X0NYG5 | Trypanosomatidae | 50% | 100% |
A0A3Q8ICN7 | Leishmania donovani | 95% | 100% |
A4HED2 | Leishmania braziliensis | 85% | 100% |
C9ZKD5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AXW1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BH15 | Trypanosoma cruzi | 49% | 100% |