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: E9B437
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.701 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 497 | 499 | PF00082 | 0.739 |
CLV_PCSK_PC1ET2_1 | 567 | 569 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.487 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.627 |
DEG_SPOP_SBC_1 | 222 | 226 | PF00917 | 0.677 |
DEG_SPOP_SBC_1 | 228 | 232 | PF00917 | 0.604 |
DEG_SPOP_SBC_1 | 476 | 480 | PF00917 | 0.605 |
DOC_CYCLIN_RxL_1 | 371 | 381 | PF00134 | 0.464 |
DOC_MAPK_gen_1 | 564 | 574 | PF00069 | 0.655 |
DOC_PP2B_LxvP_1 | 192 | 195 | PF13499 | 0.692 |
DOC_PP4_FxxP_1 | 445 | 448 | PF00568 | 0.523 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.669 |
DOC_USP7_UBL2_3 | 508 | 512 | PF12436 | 0.769 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.591 |
LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 144 | 149 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 536 | 545 | PF00244 | 0.696 |
LIG_BRCT_BRCA1_1 | 94 | 98 | PF00533 | 0.675 |
LIG_Clathr_ClatBox_1 | 286 | 290 | PF01394 | 0.630 |
LIG_eIF4E_1 | 398 | 404 | PF01652 | 0.459 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.746 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.731 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.525 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.476 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.701 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.677 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.572 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.632 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.590 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.562 |
LIG_Integrin_RGD_1 | 82 | 84 | PF01839 | 0.773 |
LIG_LIR_Apic_2 | 444 | 448 | PF02991 | 0.595 |
LIG_LIR_Apic_2 | 95 | 99 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 276 | 283 | PF02991 | 0.687 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.736 |
LIG_LIR_Nem_3 | 31 | 35 | PF02991 | 0.488 |
LIG_PCNA_yPIPBox_3 | 371 | 380 | PF02747 | 0.580 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.569 |
LIG_SH2_NCK_1 | 245 | 249 | PF00017 | 0.648 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.712 |
LIG_SH2_STAT3 | 113 | 116 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.803 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.690 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.569 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.673 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.702 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.517 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.708 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.671 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.599 |
LIG_SUMO_SIM_par_1 | 363 | 369 | PF11976 | 0.664 |
LIG_SUMO_SIM_par_1 | 375 | 381 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 550 | 557 | PF11976 | 0.656 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.615 |
LIG_TYR_ITIM | 36 | 41 | PF00017 | 0.580 |
LIG_UBA3_1 | 562 | 567 | PF00899 | 0.628 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.691 |
LIG_WRC_WIRS_1 | 412 | 417 | PF05994 | 0.536 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.744 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.692 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.624 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.578 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.596 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.664 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.642 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.626 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.687 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.761 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.678 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.569 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.712 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.473 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.607 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.651 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.711 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.695 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.797 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.518 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.535 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.629 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.634 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.683 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.533 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.704 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.565 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.632 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.649 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.703 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.637 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.616 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.655 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.668 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.722 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.711 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.553 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.660 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.635 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.635 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.614 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.597 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.675 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.542 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.538 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.774 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.672 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.509 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.439 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.577 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.615 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.539 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.585 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.678 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.767 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.592 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.492 |
MOD_PK_1 | 568 | 574 | PF00069 | 0.672 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.745 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.619 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.663 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.605 |
MOD_Plk_1 | 568 | 574 | PF00069 | 0.672 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.585 |
MOD_Plk_2-3 | 378 | 384 | PF00069 | 0.583 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.555 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.535 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.478 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.463 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.526 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.632 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.736 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.776 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.605 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.775 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.664 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.635 |
TRG_DiLeu_BaEn_2 | 283 | 289 | PF01217 | 0.510 |
TRG_DiLeu_BaLyEn_6 | 372 | 377 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 449 | 454 | PF01217 | 0.661 |
TRG_DiLeu_BaLyEn_6 | 548 | 553 | PF01217 | 0.592 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.748 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 262 | 265 | PF00400 | 0.668 |
TRG_NES_CRM1_1 | 284 | 297 | PF08389 | 0.649 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2A9 | Leptomonas seymouri | 36% | 96% |
A0A3Q8IEY7 | Leishmania donovani | 87% | 100% |
A4HLR1 | Leishmania braziliensis | 70% | 99% |
A4I961 | Leishmania infantum | 87% | 89% |
Q4Q3Y8 | Leishmania major | 86% | 98% |