Kinetoplastid-unique proteins with many disordered segments and a hydrophobic C-terminal region.
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 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HHA7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.365 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 409 | 415 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.459 |
DEG_APCC_DBOX_1 | 305 | 313 | PF00400 | 0.585 |
DEG_APCC_DBOX_1 | 55 | 63 | PF00400 | 0.687 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.588 |
DEG_SCF_SKP2-CKS1_1 | 113 | 120 | PF00560 | 0.584 |
DEG_SCF_SKP2-CKS1_1 | 165 | 172 | PF00560 | 0.575 |
DEG_SPOP_SBC_1 | 8 | 12 | PF00917 | 0.725 |
DOC_CDC14_PxL_1 | 370 | 378 | PF14671 | 0.394 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.579 |
DOC_CYCLIN_yCln2_LP_2 | 376 | 382 | PF00134 | 0.242 |
DOC_PP4_FxxP_1 | 393 | 396 | PF00568 | 0.341 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.666 |
DOC_USP7_UBL2_3 | 116 | 120 | PF12436 | 0.744 |
DOC_USP7_UBL2_3 | 131 | 135 | PF12436 | 0.677 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.593 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 321 | 326 | PF00244 | 0.576 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.733 |
LIG_deltaCOP1_diTrp_1 | 335 | 340 | PF00928 | 0.300 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.628 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.650 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.673 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.491 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.303 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.614 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.667 |
LIG_FXI_DFP_1 | 313 | 317 | PF00024 | 0.402 |
LIG_LIR_Gen_1 | 108 | 118 | PF02991 | 0.726 |
LIG_LIR_Gen_1 | 150 | 160 | PF02991 | 0.631 |
LIG_LIR_Gen_1 | 279 | 286 | PF02991 | 0.703 |
LIG_LIR_Gen_1 | 323 | 333 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 334 | 344 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.730 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.374 |
LIG_Pex14_1 | 336 | 340 | PF04695 | 0.300 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.639 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.615 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.628 |
LIG_SH2_CRK | 296 | 300 | PF00017 | 0.676 |
LIG_SH2_CRK | 32 | 36 | PF00017 | 0.735 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.335 |
LIG_SH2_GRB2like | 31 | 34 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 213 | 217 | PF00017 | 0.682 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.641 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.398 |
LIG_SH2_STAT3 | 350 | 353 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.732 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.416 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.602 |
LIG_SH3_4 | 131 | 138 | PF00018 | 0.673 |
LIG_SUMO_SIM_anti_2 | 214 | 220 | PF11976 | 0.592 |
LIG_SUMO_SIM_anti_2 | 385 | 390 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 395 | 401 | PF11976 | 0.299 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.606 |
LIG_TYR_ITIM | 294 | 299 | PF00017 | 0.677 |
LIG_TYR_ITIM | 339 | 344 | PF00017 | 0.335 |
MOD_CDK_SPK_2 | 126 | 131 | PF00069 | 0.635 |
MOD_CDK_SPK_2 | 166 | 171 | PF00069 | 0.578 |
MOD_CDK_SPxK_1 | 114 | 120 | PF00069 | 0.583 |
MOD_CDK_SPxK_1 | 166 | 172 | PF00069 | 0.581 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.436 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.716 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.704 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.718 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.456 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.515 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.440 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.556 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.569 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.576 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.686 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.669 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.608 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.300 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.662 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.716 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.792 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.400 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.674 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.681 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.331 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.715 |
MOD_NEK2_2 | 15 | 20 | PF00069 | 0.565 |
MOD_NEK2_2 | 9 | 14 | PF00069 | 0.582 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.593 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.735 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.649 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.597 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.611 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.706 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.664 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.704 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.645 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.560 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.636 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.660 |
MOD_SUMO_rev_2 | 138 | 144 | PF00179 | 0.620 |
MOD_SUMO_rev_2 | 279 | 288 | PF00179 | 0.680 |
TRG_DiLeu_BaEn_1 | 290 | 295 | PF01217 | 0.709 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.296 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.744 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.720 |
TRG_Pf-PMV_PEXEL_1 | 186 | 191 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF35 | Leptomonas seymouri | 68% | 74% |
A0A0S4JJG2 | Bodo saltans | 33% | 87% |
A0A1X0NZR0 | Trypanosomatidae | 56% | 80% |
A0A3Q8IF28 | Leishmania donovani | 81% | 73% |
A4I4F3 | Leishmania infantum | 81% | 73% |
C9ZLK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 84% |
E9ADV3 | Leishmania major | 82% | 100% |
E9ALX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 73% |