A membrane-associated protein in Kinetoplastids with quite unique helical folds.. Only expanded in the Strigomonas lineage
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:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A0A3Q8IFM0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.476 |
CLV_PCSK_FUR_1 | 103 | 107 | PF00082 | 0.437 |
CLV_PCSK_FUR_1 | 277 | 281 | PF00082 | 0.418 |
CLV_PCSK_FUR_1 | 336 | 340 | PF00082 | 0.489 |
CLV_PCSK_FUR_1 | 63 | 67 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 279 | 281 | PF00082 | 0.428 |
CLV_PCSK_PC7_1 | 276 | 282 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.483 |
CLV_Separin_Metazoa | 49 | 53 | PF03568 | 0.587 |
DEG_APCC_DBOX_1 | 136 | 144 | PF00400 | 0.608 |
DEG_SCF_FBW7_1 | 192 | 197 | PF00400 | 0.659 |
DEG_SCF_FBW7_1 | 215 | 221 | PF00400 | 0.706 |
DEG_SCF_FBW7_1 | 326 | 331 | PF00400 | 0.652 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.698 |
DOC_CKS1_1 | 325 | 330 | PF01111 | 0.683 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 112 | 119 | PF00134 | 0.669 |
DOC_MAPK_gen_1 | 133 | 140 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 262 | 271 | PF00069 | 0.632 |
DOC_MAPK_gen_1 | 42 | 50 | PF00069 | 0.605 |
DOC_MAPK_gen_1 | 63 | 73 | PF00069 | 0.586 |
DOC_MAPK_HePTP_8 | 102 | 119 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 112 | 119 | PF00069 | 0.623 |
DOC_MAPK_MEF2A_6 | 65 | 74 | PF00069 | 0.583 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.641 |
DOC_PP4_FxxP_1 | 88 | 91 | PF00568 | 0.649 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.706 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.711 |
LIG_14-3-3_CanoR_1 | 106 | 112 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 170 | 180 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 284 | 291 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 99 | 103 | PF00244 | 0.661 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.402 |
LIG_BIR_III_2 | 153 | 157 | PF00653 | 0.678 |
LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.689 |
LIG_CaM_IQ_9 | 269 | 284 | PF13499 | 0.629 |
LIG_Clathr_ClatBox_1 | 72 | 76 | PF01394 | 0.593 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.304 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.716 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.648 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.673 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.595 |
LIG_Integrin_isoDGR_2 | 146 | 148 | PF01839 | 0.444 |
LIG_LIR_Apic_2 | 85 | 91 | PF02991 | 0.694 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.713 |
LIG_SH2_GRB2like | 181 | 184 | PF00017 | 0.711 |
LIG_SH2_GRB2like | 31 | 34 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.529 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.704 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.801 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.634 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.701 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.651 |
LIG_SUMO_SIM_anti_2 | 268 | 274 | PF11976 | 0.567 |
LIG_SUMO_SIM_anti_2 | 69 | 76 | PF11976 | 0.587 |
LIG_SUMO_SIM_par_1 | 69 | 76 | PF11976 | 0.587 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.666 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.632 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.720 |
LIG_UBA3_1 | 271 | 279 | PF00899 | 0.652 |
MOD_CDK_SPxxK_3 | 317 | 324 | PF00069 | 0.645 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.372 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.672 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.716 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.600 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.720 |
MOD_Cter_Amidation | 369 | 372 | PF01082 | 0.501 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.542 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.479 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.506 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.511 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.678 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.692 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.756 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.588 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.656 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.766 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.642 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.394 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.460 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.521 |
MOD_NEK2_2 | 107 | 112 | PF00069 | 0.622 |
MOD_NEK2_2 | 328 | 333 | PF00069 | 0.724 |
MOD_NEK2_2 | 98 | 103 | PF00069 | 0.647 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.633 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.619 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.538 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.633 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.600 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.418 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.762 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.812 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.766 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.666 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.712 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.665 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.632 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.684 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.712 |
MOD_SUMO_rev_2 | 337 | 344 | PF00179 | 0.669 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.700 |
TRG_NLS_MonoExtC_3 | 280 | 285 | PF00514 | 0.625 |
TRG_NLS_MonoExtC_3 | 370 | 375 | PF00514 | 0.695 |
TRG_NLS_MonoExtN_4 | 279 | 285 | PF00514 | 0.619 |
TRG_NLS_MonoExtN_4 | 371 | 376 | PF00514 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 65 | 69 | PF00026 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HX69 | Leptomonas seymouri | 55% | 98% |
A4HJF5 | Leishmania braziliensis | 65% | 99% |
A4I6V0 | Leishmania infantum | 100% | 100% |
E9B1X3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4Q689 | Leishmania major | 88% | 100% |