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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B615
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.690 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.752 |
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.505 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.460 |
CLV_PCSK_FUR_1 | 426 | 430 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.527 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.589 |
DEG_SCF_FBW7_1 | 361 | 367 | PF00400 | 0.656 |
DEG_SPOP_SBC_1 | 201 | 205 | PF00917 | 0.728 |
DOC_CKS1_1 | 245 | 250 | PF01111 | 0.663 |
DOC_CKS1_1 | 361 | 366 | PF01111 | 0.658 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.699 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.630 |
DOC_USP7_UBL2_3 | 396 | 400 | PF12436 | 0.526 |
DOC_USP7_UBL2_3 | 60 | 64 | PF12436 | 0.688 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.698 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 49 | 58 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 82 | 91 | PF00244 | 0.554 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.563 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.364 |
LIG_eIF4E_1 | 323 | 329 | PF01652 | 0.599 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.682 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.562 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.634 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.652 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.642 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.656 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.533 |
LIG_LIR_Gen_1 | 377 | 385 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.748 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.525 |
LIG_Pex14_2 | 58 | 62 | PF04695 | 0.656 |
LIG_SH2_GRB2like | 323 | 326 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.659 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.599 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.630 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.678 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.660 |
LIG_SUMO_SIM_anti_2 | 377 | 384 | PF11976 | 0.517 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.565 |
LIG_UBA3_1 | 398 | 407 | PF00899 | 0.409 |
MOD_CDK_SPK_2 | 360 | 365 | PF00069 | 0.657 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.511 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.674 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.568 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.652 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.673 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.583 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.655 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.681 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.661 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.562 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.662 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.714 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.732 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.620 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.639 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.701 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.577 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.597 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.586 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.635 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.651 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.623 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.568 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.700 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.509 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.651 |
MOD_LATS_1 | 47 | 53 | PF00433 | 0.659 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.563 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.426 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.755 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.713 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.533 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.692 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.691 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.573 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.636 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.702 |
MOD_PK_1 | 19 | 25 | PF00069 | 0.584 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.602 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.591 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.692 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.653 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.665 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.610 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.600 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.633 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.608 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.495 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.474 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.538 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.599 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.531 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.660 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.610 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.644 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.517 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.698 |
MOD_SUMO_rev_2 | 381 | 391 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_1 | 394 | 399 | PF01217 | 0.364 |
TRG_DiLeu_BaEn_2 | 386 | 392 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_3 | 377 | 383 | PF01217 | 0.472 |
TRG_DiLeu_LyEn_5 | 394 | 399 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.604 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 395 | 398 | PF00400 | 0.484 |
TRG_NLS_MonoExtC_3 | 297 | 302 | PF00514 | 0.650 |
TRG_NLS_MonoExtN_4 | 296 | 302 | PF00514 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 322 | 326 | PF00026 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IV47 | Leishmania donovani | 83% | 100% |
A4HMF8 | Leishmania braziliensis | 54% | 100% |
A4IB29 | Leishmania infantum | 83% | 100% |
E9AEV9 | Leishmania major | 81% | 100% |