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: 2, no: 4 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H5N7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.814 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.773 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.685 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.815 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 469 | 471 | PF00082 | 0.563 |
CLV_PCSK_PC7_1 | 432 | 438 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.626 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.558 |
DOC_CYCLIN_yCln2_LP_2 | 285 | 291 | PF00134 | 0.660 |
DOC_MAPK_gen_1 | 388 | 397 | PF00069 | 0.538 |
DOC_PP2B_LxvP_1 | 285 | 288 | PF13499 | 0.657 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.836 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.541 |
DOC_USP7_UBL2_3 | 337 | 341 | PF12436 | 0.533 |
DOC_USP7_UBL2_3 | 410 | 414 | PF12436 | 0.581 |
DOC_USP7_UBL2_3 | 417 | 421 | PF12436 | 0.683 |
DOC_USP7_UBL2_3 | 449 | 453 | PF12436 | 0.648 |
DOC_USP7_UBL2_3 | 460 | 464 | PF12436 | 0.569 |
DOC_USP7_UBL2_3 | 480 | 484 | PF12436 | 0.624 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 247 | 255 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 308 | 314 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.741 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.482 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.495 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.550 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.533 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.519 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.746 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.565 |
LIG_Integrin_RGD_1 | 272 | 274 | PF01839 | 0.522 |
LIG_NRBOX | 1 | 7 | PF00104 | 0.461 |
LIG_NRP_CendR_1 | 492 | 494 | PF00754 | 0.551 |
LIG_PCNA_yPIPBox_3 | 104 | 112 | PF02747 | 0.511 |
LIG_Pex14_2 | 25 | 29 | PF04695 | 0.537 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.478 |
LIG_SH3_1 | 471 | 477 | PF00018 | 0.552 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.483 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.672 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.667 |
LIG_SH3_4 | 372 | 379 | PF00018 | 0.560 |
LIG_SH3_4 | 449 | 456 | PF00018 | 0.712 |
LIG_SUMO_SIM_anti_2 | 122 | 128 | PF11976 | 0.599 |
MOD_CDC14_SPxK_1 | 359 | 362 | PF00782 | 0.542 |
MOD_CDK_SPxK_1 | 356 | 362 | PF00069 | 0.550 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.664 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.534 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.569 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.424 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.709 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.605 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.689 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.551 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.606 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.531 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.443 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.659 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.560 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.540 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.525 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.656 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.604 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.704 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.562 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.744 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.444 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.591 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.656 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.587 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.523 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.601 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.522 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.711 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.662 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.763 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.663 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.662 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.602 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.569 |
MOD_LATS_1 | 343 | 349 | PF00433 | 0.570 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.515 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.434 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.620 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.671 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.479 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.434 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.604 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.514 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.543 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.692 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.458 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.473 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.628 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.520 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.574 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.627 |
MOD_PKA_1 | 452 | 458 | PF00069 | 0.703 |
MOD_PKA_1 | 469 | 475 | PF00069 | 0.566 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.530 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.435 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.716 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.672 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.619 |
MOD_PKB_1 | 167 | 175 | PF00069 | 0.533 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.682 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.604 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.436 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.682 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.659 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.568 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.458 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.523 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.481 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.586 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.566 |
MOD_SUMO_for_1 | 214 | 217 | PF00179 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 319 | 324 | PF01217 | 0.490 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.566 |
TRG_NLS_Bipartite_1 | 452 | 473 | PF00514 | 0.560 |
TRG_NLS_MonoExtC_3 | 459 | 464 | PF00514 | 0.566 |
TRG_NLS_MonoExtN_4 | 414 | 420 | PF00514 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.586 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILW1 | Leptomonas seymouri | 43% | 96% |
A0A3Q8I7H5 | Leishmania donovani | 65% | 100% |
A4HU09 | Leishmania infantum | 65% | 100% |
E9AMT9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 96% |
Q4QHT6 | Leishmania major | 58% | 93% |