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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q9BHF0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 208 | 212 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.645 |
CLV_PCSK_PC7_1 | 377 | 383 | PF00082 | 0.449 |
CLV_PCSK_PC7_1 | 78 | 84 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.579 |
CLV_Separin_Metazoa | 72 | 76 | PF03568 | 0.419 |
DEG_APCC_DBOX_1 | 336 | 344 | PF00400 | 0.446 |
DEG_SPOP_SBC_1 | 168 | 172 | PF00917 | 0.408 |
DOC_CKS1_1 | 440 | 445 | PF01111 | 0.667 |
DOC_MAPK_gen_1 | 175 | 183 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 175 | 183 | PF00069 | 0.480 |
DOC_MIT_MIM_1 | 117 | 125 | PF04212 | 0.337 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.606 |
DOC_USP7_UBL2_3 | 286 | 290 | PF12436 | 0.489 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.773 |
LIG_14-3-3_CanoR_1 | 216 | 226 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 312 | 316 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 332 | 350 | PF00022 | 0.444 |
LIG_APCC_ABBAyCdc20_2 | 176 | 182 | PF00400 | 0.506 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.447 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.429 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.357 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.763 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.507 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.586 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.529 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.480 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.652 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.843 |
LIG_IRF3_LxIS_1 | 363 | 368 | PF10401 | 0.501 |
LIG_NRBOX | 69 | 75 | PF00104 | 0.416 |
LIG_PCNA_PIPBox_1 | 133 | 142 | PF02747 | 0.489 |
LIG_Pex14_1 | 324 | 328 | PF04695 | 0.471 |
LIG_SH2_PTP2 | 180 | 183 | PF00017 | 0.506 |
LIG_SH2_SRC | 180 | 183 | PF00017 | 0.506 |
LIG_SH2_STAT3 | 113 | 116 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 139 | 142 | PF00017 | 0.491 |
LIG_SH2_STAT3 | 376 | 379 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.507 |
LIG_SH3_1 | 327 | 333 | PF00018 | 0.463 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.497 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.484 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.568 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.432 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.405 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.677 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.789 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.803 |
LIG_SUMO_SIM_par_1 | 355 | 360 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 362 | 368 | PF11976 | 0.376 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.581 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.818 |
LIG_TRAF2_1 | 445 | 448 | PF00917 | 0.585 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.429 |
LIG_UBA3_1 | 364 | 372 | PF00899 | 0.360 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.562 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.699 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.702 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.754 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.516 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.755 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.675 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.562 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.776 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.568 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.528 |
MOD_Cter_Amidation | 173 | 176 | PF01082 | 0.503 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.755 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.549 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.573 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.576 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.765 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.649 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.453 |
MOD_GlcNHglycan | 7 | 11 | PF01048 | 0.751 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.647 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.569 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.577 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.709 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.676 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.689 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.745 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.761 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.572 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.662 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.620 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.711 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.680 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.574 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.473 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.401 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.675 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.742 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.567 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.621 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.720 |
MOD_PKA_1 | 380 | 386 | PF00069 | 0.574 |
MOD_PKA_1 | 82 | 88 | PF00069 | 0.411 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.588 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.751 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.587 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.616 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.585 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.588 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.473 |
MOD_PKB_1 | 229 | 237 | PF00069 | 0.683 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.723 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.590 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.634 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.725 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.640 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.450 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.725 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.600 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.544 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.719 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.714 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.700 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.762 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.728 |
MOD_SUMO_rev_2 | 224 | 234 | PF00179 | 0.576 |
TRG_DiLeu_BaLyEn_6 | 131 | 136 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.718 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBU0 | Leptomonas seymouri | 46% | 99% |
A0A3S7X462 | Leishmania donovani | 87% | 100% |
A4HJ39 | Leishmania braziliensis | 70% | 100% |
A4I6F4 | Leishmania infantum | 87% | 100% |
C9ZN69 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9B1L1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |