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: E9AW74
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.819 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.365 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.470 |
CLV_PCSK_PC7_1 | 379 | 385 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.450 |
DEG_APCC_DBOX_1 | 55 | 63 | PF00400 | 0.314 |
DOC_CKS1_1 | 292 | 297 | PF01111 | 0.731 |
DOC_MAPK_gen_1 | 79 | 85 | PF00069 | 0.632 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.388 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.312 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.650 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.764 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 182 | 187 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 255 | 263 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 290 | 295 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 298 | 304 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 357 | 361 | PF00244 | 0.790 |
LIG_14-3-3_CanoR_1 | 6 | 11 | PF00244 | 0.400 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.312 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.545 |
LIG_BRCT_BRCA1_1 | 257 | 261 | PF00533 | 0.740 |
LIG_EH1_1 | 22 | 30 | PF00400 | 0.302 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.604 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.698 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.342 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.732 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.708 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.651 |
LIG_GBD_Chelix_1 | 17 | 25 | PF00786 | 0.312 |
LIG_GBD_Chelix_1 | 66 | 74 | PF00786 | 0.340 |
LIG_Integrin_RGD_1 | 340 | 342 | PF01839 | 0.519 |
LIG_LIR_Apic_2 | 289 | 295 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 258 | 268 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 35 | 41 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.340 |
LIG_Pex14_1 | 69 | 73 | PF04695 | 0.312 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.729 |
LIG_SH2_NCK_1 | 153 | 157 | PF00017 | 0.587 |
LIG_SH2_NCK_1 | 292 | 296 | PF00017 | 0.781 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.811 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.312 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.703 |
LIG_WRC_WIRS_1 | 183 | 188 | PF05994 | 0.485 |
MOD_CDK_SPxxK_3 | 291 | 298 | PF00069 | 0.673 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.640 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.439 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.548 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.766 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.560 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.674 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.589 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.638 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.641 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.522 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.526 |
MOD_Cter_Amidation | 381 | 384 | PF01082 | 0.581 |
MOD_GlcNHglycan | 105 | 110 | PF01048 | 0.570 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.771 |
MOD_GlcNHglycan | 138 | 142 | PF01048 | 0.551 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.718 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.640 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.621 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.628 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.550 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.790 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.564 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.660 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.655 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.651 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.614 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.613 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.538 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.677 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.556 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.644 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.559 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.715 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.772 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.691 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.511 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.794 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.643 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.517 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.406 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.406 |
MOD_N-GLC_2 | 52 | 54 | PF02516 | 0.464 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.633 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.348 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.605 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.436 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.537 |
MOD_PK_1 | 255 | 261 | PF00069 | 0.632 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.560 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.592 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.647 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.573 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.751 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.592 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.514 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.647 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.653 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.774 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.686 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.563 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.637 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.408 |
MOD_Plk_2-3 | 279 | 285 | PF00069 | 0.587 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.637 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.625 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.726 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.644 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.719 |
MOD_SUMO_rev_2 | 46 | 51 | PF00179 | 0.406 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.445 |
TRG_ER_diLys_1 | 405 | 409 | PF00400 | 0.644 |
TRG_NES_CRM1_1 | 276 | 287 | PF08389 | 0.665 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 79 | 84 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ47 | Leptomonas seymouri | 34% | 96% |
A0A3Q8IEI6 | Leishmania donovani | 86% | 100% |
A4H6H5 | Leishmania braziliensis | 65% | 100% |
A4I0B0 | Leishmania infantum | 87% | 100% |
Q9NF81 | Leishmania major | 84% | 100% |