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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AX04
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.685 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.688 |
CLV_PCSK_FUR_1 | 378 | 382 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.682 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.730 |
CLV_PCSK_PC7_1 | 373 | 379 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.667 |
CLV_Separin_Metazoa | 162 | 166 | PF03568 | 0.450 |
DEG_APCC_DBOX_1 | 525 | 533 | PF00400 | 0.612 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.575 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.607 |
DEG_SCF_TRCP1_1 | 248 | 253 | PF00400 | 0.321 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 518 | 527 | PF00134 | 0.603 |
DOC_MAPK_MEF2A_6 | 145 | 152 | PF00069 | 0.426 |
DOC_MAPK_NFAT4_5 | 145 | 153 | PF00069 | 0.431 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.523 |
DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.775 |
DOC_PP2B_LxvP_1 | 436 | 439 | PF13499 | 0.517 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.681 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 149 | 153 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 283 | 292 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 330 | 340 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 343 | 349 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 362 | 368 | PF00244 | 0.512 |
LIG_Actin_WH2_2 | 360 | 375 | PF00022 | 0.751 |
LIG_Actin_WH2_2 | 8 | 26 | PF00022 | 0.598 |
LIG_deltaCOP1_diTrp_1 | 166 | 175 | PF00928 | 0.420 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.592 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.713 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.700 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.539 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.524 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.626 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.768 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.683 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.647 |
LIG_GBD_Chelix_1 | 50 | 58 | PF00786 | 0.552 |
LIG_LIR_Gen_1 | 166 | 177 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.524 |
LIG_LYPXL_yS_3 | 19 | 22 | PF13949 | 0.550 |
LIG_MYND_1 | 309 | 313 | PF01753 | 0.641 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.583 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.608 |
LIG_SH2_STAT3 | 256 | 259 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.455 |
LIG_SH3_2 | 37 | 42 | PF14604 | 0.506 |
LIG_SH3_2 | 439 | 444 | PF14604 | 0.528 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.467 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.636 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.646 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.534 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.720 |
LIG_SUMO_SIM_anti_2 | 193 | 198 | PF11976 | 0.533 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 386 | 396 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 78 | 84 | PF11976 | 0.448 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.515 |
MOD_CDK_SPxxK_3 | 492 | 499 | PF00069 | 0.635 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.528 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.542 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.739 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.655 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.823 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.525 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.800 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.821 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.546 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.748 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.685 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.447 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.632 |
MOD_CMANNOS | 528 | 531 | PF00535 | 0.683 |
MOD_DYRK1A_RPxSP_1 | 297 | 301 | PF00069 | 0.502 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.507 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.600 |
MOD_GlcNHglycan | 247 | 251 | PF01048 | 0.602 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.483 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.550 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.597 |
MOD_GlcNHglycan | 46 | 50 | PF01048 | 0.616 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.814 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.495 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.502 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.731 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.819 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.718 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.643 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.843 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.833 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.509 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.791 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.673 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.643 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.573 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.434 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.619 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.716 |
MOD_N-GLC_2 | 414 | 416 | PF02516 | 0.612 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.500 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.352 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.332 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.541 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.534 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.631 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.618 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.502 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.458 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.501 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.731 |
MOD_PK_1 | 63 | 69 | PF00069 | 0.456 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.527 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.523 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.632 |
MOD_PKB_1 | 120 | 128 | PF00069 | 0.463 |
MOD_PKB_1 | 379 | 387 | PF00069 | 0.821 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.608 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.819 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.568 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.357 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.482 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.562 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.794 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.662 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.664 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.754 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.760 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.639 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.682 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.528 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 523 | 526 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 543 | 546 | PF00400 | 0.545 |
TRG_NES_CRM1_1 | 317 | 329 | PF08389 | 0.695 |
TRG_NLS_MonoCore_2 | 375 | 380 | PF00514 | 0.726 |
TRG_NLS_MonoExtC_3 | 375 | 380 | PF00514 | 0.828 |
TRG_NLS_MonoExtN_4 | 373 | 380 | PF00514 | 0.728 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7U6 | Leptomonas seymouri | 44% | 80% |
A0A3S7WYG0 | Leishmania donovani | 83% | 100% |
A4HDL9 | Leishmania braziliensis | 67% | 100% |
E9AH66 | Leishmania infantum | 84% | 100% |
Q4QAH2 | Leishmania major | 82% | 100% |