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: A0A3S7X462
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 208 | 212 | PF00656 | 0.528 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.569 |
CLV_PCSK_FUR_1 | 229 | 233 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.652 |
CLV_PCSK_PC7_1 | 78 | 84 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.652 |
CLV_Separin_Metazoa | 72 | 76 | PF03568 | 0.421 |
DEG_APCC_DBOX_1 | 336 | 344 | PF00400 | 0.447 |
DOC_MAPK_gen_1 | 175 | 183 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 288 | 297 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 33 | 43 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 175 | 183 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.337 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.385 |
DOC_USP7_UBL2_3 | 286 | 290 | PF12436 | 0.501 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 312 | 316 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.519 |
LIG_Actin_WH2_2 | 332 | 350 | PF00022 | 0.444 |
LIG_APCC_ABBAyCdc20_2 | 176 | 182 | PF00400 | 0.504 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.466 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.411 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.429 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.350 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.818 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.509 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.594 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.558 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.479 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.840 |
LIG_IRF3_LxIS_1 | 363 | 368 | PF10401 | 0.501 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.437 |
LIG_NRBOX | 121 | 127 | PF00104 | 0.334 |
LIG_NRBOX | 69 | 75 | PF00104 | 0.419 |
LIG_PCNA_PIPBox_1 | 133 | 142 | PF02747 | 0.490 |
LIG_PDZ_Class_3 | 453 | 458 | PF00595 | 0.724 |
LIG_Pex14_1 | 324 | 328 | PF04695 | 0.471 |
LIG_SH2_PTP2 | 180 | 183 | PF00017 | 0.494 |
LIG_SH2_SRC | 180 | 183 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 113 | 116 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 139 | 142 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.480 |
LIG_SH3_1 | 327 | 333 | PF00018 | 0.464 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.522 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.568 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.449 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.384 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.669 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.784 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.794 |
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 | 0.573 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.813 |
LIG_TRAF2_1 | 445 | 448 | PF00917 | 0.751 |
LIG_UBA3_1 | 364 | 372 | PF00899 | 0.360 |
MOD_CDC14_SPxK_1 | 108 | 111 | PF00782 | 0.535 |
MOD_CDK_SPxK_1 | 105 | 111 | PF00069 | 0.549 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.670 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.698 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.628 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.778 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.769 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.666 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.771 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.698 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.731 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.529 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.524 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.532 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.738 |
MOD_GlcNHglycan | 7 | 11 | PF01048 | 0.703 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.573 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.633 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.663 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.666 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.741 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.672 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.781 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.672 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.579 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.561 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.728 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.665 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.524 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.504 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.369 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.674 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.705 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.572 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.585 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.699 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.518 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.742 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.647 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.616 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.612 |
MOD_PKB_1 | 229 | 237 | PF00069 | 0.663 |
MOD_PKB_1 | 378 | 386 | PF00069 | 0.570 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.786 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.552 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.786 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.635 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.448 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.516 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.646 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.494 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.736 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.704 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.691 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.761 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.579 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.638 |
TRG_DiLeu_BaLyEn_6 | 131 | 136 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.721 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBU0 | Leptomonas seymouri | 44% | 99% |
A4HJ39 | Leishmania braziliensis | 70% | 98% |
A4I6F4 | Leishmania infantum | 100% | 100% |
C9ZN69 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9B1L1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q9BHF0 | Leishmania major | 87% | 100% |