Unique kinetoplastid membrane protein. Protein duplicated in Leishmanniids as well as in T. rangeli.
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: A4H6H5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.816 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.845 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.526 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.695 |
DEG_SPOP_SBC_1 | 342 | 346 | PF00917 | 0.665 |
DOC_ANK_TNKS_1 | 380 | 387 | PF00023 | 0.671 |
DOC_CKS1_1 | 290 | 295 | PF01111 | 0.831 |
DOC_MAPK_gen_1 | 79 | 85 | PF00069 | 0.724 |
DOC_PP1_RVXF_1 | 89 | 96 | PF00149 | 0.563 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.397 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.819 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.818 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.815 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.800 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.828 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.674 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 234 | 240 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 288 | 293 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 343 | 349 | PF00244 | 0.734 |
LIG_14-3-3_CterR_2 | 403 | 407 | PF00244 | 0.656 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.411 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.641 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.846 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.659 |
LIG_eIF4E_1 | 61 | 67 | PF01652 | 0.261 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.436 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.261 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.628 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.667 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.844 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.727 |
LIG_GBD_Chelix_1 | 17 | 25 | PF00786 | 0.411 |
LIG_LIR_Apic_2 | 256 | 262 | PF02991 | 0.820 |
LIG_LIR_Apic_2 | 287 | 293 | PF02991 | 0.744 |
LIG_LIR_Gen_1 | 35 | 41 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.632 |
LIG_Pex14_1 | 355 | 359 | PF04695 | 0.629 |
LIG_Pex14_1 | 69 | 73 | PF04695 | 0.411 |
LIG_Pex14_2 | 359 | 363 | PF04695 | 0.633 |
LIG_Pex14_2 | 59 | 63 | PF04695 | 0.290 |
LIG_PTB_Apo_2 | 30 | 37 | PF02174 | 0.330 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.829 |
LIG_SH2_NCK_1 | 290 | 294 | PF00017 | 0.829 |
LIG_SH2_STAT3 | 321 | 324 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.792 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.826 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.411 |
MOD_CDK_SPK_2 | 196 | 201 | PF00069 | 0.662 |
MOD_CDK_SPxK_1 | 223 | 229 | PF00069 | 0.653 |
MOD_CDK_SPxxK_3 | 196 | 203 | PF00069 | 0.664 |
MOD_CDK_SPxxK_3 | 289 | 296 | PF00069 | 0.832 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.681 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.815 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.642 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.656 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.754 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.719 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.777 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.693 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.610 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.675 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.776 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.663 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.690 |
MOD_Cter_Amidation | 116 | 119 | PF01082 | 0.603 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.468 |
MOD_GlcNHglycan | 138 | 142 | PF01048 | 0.519 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.461 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.542 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.604 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.507 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.534 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.503 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.635 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.566 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.557 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.591 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.782 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.740 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.680 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.833 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.683 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.776 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.830 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.741 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.835 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.732 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.801 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.647 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.573 |
MOD_LATS_1 | 341 | 347 | PF00433 | 0.665 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.637 |
MOD_N-GLC_2 | 52 | 54 | PF02516 | 0.689 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.611 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.657 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.686 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.299 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.726 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.741 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.513 |
MOD_PKA_1 | 127 | 133 | PF00069 | 0.735 |
MOD_PKA_1 | 179 | 185 | PF00069 | 0.717 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.743 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.706 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.766 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.779 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.833 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.610 |
MOD_PKB_1 | 232 | 240 | PF00069 | 0.651 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.728 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.437 |
MOD_Plk_2-3 | 277 | 283 | PF00069 | 0.746 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.750 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.308 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.589 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.717 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.671 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.798 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.831 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.675 |
MOD_SUMO_rev_2 | 46 | 51 | PF00179 | 0.440 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.765 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.792 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.726 |
TRG_NES_CRM1_1 | 274 | 285 | PF08389 | 0.823 |
TRG_Pf-PMV_PEXEL_1 | 186 | 190 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ47 | Leptomonas seymouri | 36% | 95% |
A0A3Q8IEI6 | Leishmania donovani | 64% | 99% |
A4I0B0 | Leishmania infantum | 64% | 99% |
E9AW74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q9NF81 | Leishmania major | 64% | 100% |