Unique kinetoplastid membrane protein. Protein duplicated in Leishmanniids as well as in T. rangeli.
Uncharacterized Protein, Uncharacterized
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 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4I0B0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.828 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.365 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.483 |
CLV_PCSK_PC7_1 | 118 | 124 | PF00082 | 0.436 |
CLV_PCSK_PC7_1 | 380 | 386 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.450 |
DEG_APCC_DBOX_1 | 55 | 63 | PF00400 | 0.314 |
DEG_COP1_1 | 259 | 267 | PF00400 | 0.631 |
DOC_CKS1_1 | 293 | 298 | PF01111 | 0.734 |
DOC_CYCLIN_yCln2_LP_2 | 10 | 16 | PF00134 | 0.255 |
DOC_MAPK_gen_1 | 79 | 85 | PF00069 | 0.639 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.388 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.312 |
DOC_PP4_FxxP_1 | 262 | 265 | PF00568 | 0.709 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.785 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 182 | 187 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 291 | 296 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 299 | 305 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 358 | 362 | PF00244 | 0.793 |
LIG_14-3-3_CanoR_1 | 380 | 386 | PF00244 | 0.658 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.312 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.727 |
LIG_EH1_1 | 22 | 30 | PF00400 | 0.302 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.701 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.342 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.740 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.700 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.646 |
LIG_GBD_Chelix_1 | 17 | 25 | PF00786 | 0.312 |
LIG_GBD_Chelix_1 | 66 | 74 | PF00786 | 0.340 |
LIG_Integrin_RGD_1 | 341 | 343 | PF01839 | 0.515 |
LIG_LIR_Apic_2 | 259 | 265 | PF02991 | 0.708 |
LIG_LIR_Gen_1 | 35 | 41 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.341 |
LIG_Pex14_1 | 69 | 73 | PF04695 | 0.312 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.733 |
LIG_SH2_NCK_1 | 293 | 297 | PF00017 | 0.785 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.706 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.816 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.312 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.673 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.689 |
MOD_CDK_SPxxK_3 | 292 | 299 | PF00069 | 0.677 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.633 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.553 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.753 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.714 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.681 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.587 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.350 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.636 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.630 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.626 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.513 |
MOD_Cter_Amidation | 116 | 119 | PF01082 | 0.630 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.524 |
MOD_GlcNHglycan | 105 | 110 | PF01048 | 0.585 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.769 |
MOD_GlcNHglycan | 138 | 142 | PF01048 | 0.557 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.593 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.699 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.645 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.671 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.622 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.641 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.791 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.656 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.657 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.640 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.627 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.546 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.672 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.567 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.650 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.564 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.691 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.763 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.796 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.648 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.584 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.709 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.417 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.403 |
MOD_N-GLC_2 | 52 | 54 | PF02516 | 0.467 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.606 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.516 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.348 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.451 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.614 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.436 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.541 |
MOD_PK_1 | 256 | 262 | PF00069 | 0.615 |
MOD_PKA_1 | 118 | 124 | PF00069 | 0.568 |
MOD_PKA_1 | 182 | 188 | PF00069 | 0.569 |
MOD_PKA_1 | 384 | 390 | PF00069 | 0.560 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.581 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.599 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.621 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.560 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.754 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.579 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.645 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.643 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.777 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.687 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.399 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.571 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.630 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.405 |
MOD_Plk_2-3 | 280 | 286 | PF00069 | 0.585 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.636 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.628 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.731 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.633 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.724 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.657 |
MOD_SUMO_rev_2 | 46 | 51 | PF00179 | 0.420 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 234 | 237 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.446 |
TRG_ER_diLys_1 | 406 | 410 | PF00400 | 0.610 |
TRG_NES_CRM1_1 | 277 | 288 | PF08389 | 0.662 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 79 | 84 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ47 | Leptomonas seymouri | 36% | 96% |
A0A3Q8IEI6 | Leishmania donovani | 100% | 100% |
A4H6H5 | Leishmania braziliensis | 64% | 99% |
E9AW74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q9NF81 | Leishmania major | 90% | 100% |