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: E9AX31
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.721 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.721 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.346 |
DEG_APCC_DBOX_1 | 461 | 469 | PF00400 | 0.524 |
DOC_CKS1_1 | 105 | 110 | PF01111 | 0.734 |
DOC_CKS1_1 | 153 | 158 | PF01111 | 0.669 |
DOC_CYCLIN_yCln2_LP_2 | 332 | 338 | PF00134 | 0.638 |
DOC_CYCLIN_yCln2_LP_2 | 87 | 90 | PF00134 | 0.525 |
DOC_MAPK_gen_1 | 445 | 453 | PF00069 | 0.499 |
DOC_PP1_RVXF_1 | 398 | 404 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 15 | 18 | PF13499 | 0.654 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.658 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.317 |
DOC_USP7_MATH_2 | 295 | 301 | PF00917 | 0.688 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 109 | 118 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 285 | 291 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 38 | 42 | PF00244 | 0.620 |
LIG_14-3-3_CterR_2 | 516 | 520 | PF00244 | 0.663 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.638 |
LIG_EH1_1 | 490 | 498 | PF00400 | 0.396 |
LIG_eIF4E_1 | 326 | 332 | PF01652 | 0.518 |
LIG_EVH1_1 | 15 | 19 | PF00568 | 0.654 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.757 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.634 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.661 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.673 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.713 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.558 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.673 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.517 |
LIG_FHA_2 | 49 | 55 | PF00498 | 0.702 |
LIG_LIR_Gen_1 | 490 | 497 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.607 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.649 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.658 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 153 | 157 | PF00017 | 0.649 |
LIG_SH2_NCK_1 | 26 | 30 | PF00017 | 0.538 |
LIG_SH2_NCK_1 | 326 | 330 | PF00017 | 0.519 |
LIG_SH2_STAT3 | 346 | 349 | PF00017 | 0.593 |
LIG_SH3_1 | 13 | 19 | PF00018 | 0.592 |
LIG_SH3_2 | 16 | 21 | PF14604 | 0.662 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.692 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.635 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.673 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.692 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.556 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.664 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.612 |
LIG_SUMO_SIM_par_1 | 367 | 375 | PF11976 | 0.633 |
LIG_TRAF2_1 | 458 | 461 | PF00917 | 0.404 |
LIG_TRAF2_1 | 464 | 467 | PF00917 | 0.384 |
LIG_UBA3_1 | 450 | 459 | PF00899 | 0.399 |
LIG_WW_1 | 23 | 26 | PF00397 | 0.652 |
LIG_WW_3 | 22 | 26 | PF00397 | 0.681 |
MOD_CDC14_SPxK_1 | 45 | 48 | PF00782 | 0.685 |
MOD_CDK_SPK_2 | 104 | 109 | PF00069 | 0.676 |
MOD_CDK_SPK_2 | 48 | 53 | PF00069 | 0.671 |
MOD_CDK_SPxK_1 | 19 | 25 | PF00069 | 0.634 |
MOD_CDK_SPxK_1 | 42 | 48 | PF00069 | 0.682 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.678 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.542 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.751 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.716 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.612 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.651 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.604 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.697 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.712 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.623 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.520 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.656 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.528 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.648 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.571 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.721 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.567 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.486 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.656 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.770 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.473 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.674 |
MOD_GlcNHglycan | 136 | 140 | PF01048 | 0.643 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.447 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.817 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.652 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.689 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.761 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.706 |
MOD_GlcNHglycan | 412 | 416 | PF01048 | 0.673 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.471 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.364 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.708 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.683 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.587 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.756 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.712 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.796 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.549 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.698 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.768 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.641 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.587 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.688 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.622 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.597 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.680 |
MOD_LATS_1 | 291 | 297 | PF00433 | 0.689 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.695 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.599 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.609 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.644 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.756 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.566 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.432 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.549 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.623 |
MOD_NEK2_2 | 377 | 382 | PF00069 | 0.651 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.688 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.687 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.644 |
MOD_PIKK_1 | 362 | 368 | PF00454 | 0.642 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.715 |
MOD_PKA_1 | 354 | 360 | PF00069 | 0.630 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.617 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.594 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.677 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.693 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.799 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.537 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.699 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.584 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.551 |
MOD_PKB_1 | 284 | 292 | PF00069 | 0.629 |
MOD_PKB_1 | 409 | 417 | PF00069 | 0.628 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.687 |
MOD_Plk_2-3 | 168 | 174 | PF00069 | 0.672 |
MOD_Plk_2-3 | 509 | 515 | PF00069 | 0.539 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.691 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.716 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.653 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.723 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.698 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.655 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.567 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.694 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.556 |
MOD_SUMO_for_1 | 458 | 461 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 81 | 87 | PF00179 | 0.714 |
TRG_DiLeu_BaEn_1 | 423 | 428 | PF01217 | 0.661 |
TRG_DiLeu_BaEn_1 | 492 | 497 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_2 | 398 | 404 | PF01217 | 0.545 |
TRG_DiLeu_BaEn_4 | 460 | 466 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 502 | 507 | PF01217 | 0.636 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.658 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.613 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ID03 | Leishmania donovani | 83% | 97% |
A4HDP7 | Leishmania braziliensis | 50% | 99% |
A4I0Z3 | Leishmania infantum | 83% | 97% |
Q4QAE5 | Leishmania major | 80% | 100% |