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: A0A3Q8IEY7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.691 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 497 | 499 | PF00082 | 0.757 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 563 | 565 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.583 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.587 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.564 |
DEG_SPOP_SBC_1 | 220 | 224 | PF00917 | 0.692 |
DEG_SPOP_SBC_1 | 228 | 232 | PF00917 | 0.596 |
DOC_CDC14_PxL_1 | 448 | 456 | PF14671 | 0.562 |
DOC_CYCLIN_RxL_1 | 371 | 381 | PF00134 | 0.481 |
DOC_MAPK_gen_1 | 560 | 570 | PF00069 | 0.714 |
DOC_PP2B_LxvP_1 | 192 | 195 | PF13499 | 0.680 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.710 |
DOC_USP7_UBL2_3 | 504 | 508 | PF12436 | 0.786 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 122 | 127 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 311 | 320 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 532 | 541 | PF00244 | 0.697 |
LIG_BRCT_BRCA1_1 | 94 | 98 | PF00533 | 0.641 |
LIG_Clathr_ClatBox_1 | 286 | 290 | PF01394 | 0.670 |
LIG_eIF4E_1 | 398 | 404 | PF01652 | 0.473 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.718 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.779 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.524 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.460 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.669 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.704 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.576 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.648 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.606 |
LIG_Integrin_RGD_1 | 82 | 84 | PF01839 | 0.768 |
LIG_LIR_Apic_2 | 447 | 452 | PF02991 | 0.625 |
LIG_LIR_Apic_2 | 95 | 99 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 276 | 283 | PF02991 | 0.698 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.752 |
LIG_LIR_Nem_3 | 31 | 35 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 444 | 448 | PF02991 | 0.541 |
LIG_PCNA_yPIPBox_3 | 371 | 380 | PF02747 | 0.582 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.579 |
LIG_SH2_NCK_1 | 245 | 249 | PF00017 | 0.653 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.653 |
LIG_SH2_STAT3 | 113 | 116 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.745 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.602 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.701 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.764 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.713 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.682 |
LIG_SUMO_SIM_par_1 | 363 | 369 | PF11976 | 0.669 |
LIG_SUMO_SIM_par_1 | 375 | 381 | PF11976 | 0.468 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.623 |
LIG_TYR_ITIM | 36 | 41 | PF00017 | 0.591 |
LIG_UBA3_1 | 558 | 563 | PF00899 | 0.719 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.690 |
LIG_WRC_WIRS_1 | 412 | 417 | PF05994 | 0.536 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.662 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.705 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.630 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.622 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.628 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.705 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.664 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.656 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.616 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.503 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.705 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.568 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.714 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.458 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.499 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.649 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.709 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.658 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.743 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.755 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.486 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.387 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.633 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.669 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.704 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.520 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.661 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.556 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.667 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.617 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.600 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.713 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.618 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.661 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.536 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.625 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.648 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.671 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.732 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.529 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.727 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.506 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.641 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.510 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.620 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.667 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.593 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.752 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.713 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.552 |
MOD_N-GLC_1 | 564 | 569 | PF02516 | 0.535 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.747 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.638 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.666 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.464 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.469 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.570 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.592 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.502 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.676 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.770 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.457 |
MOD_PK_1 | 564 | 570 | PF00069 | 0.709 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.772 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.587 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.523 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.716 |
MOD_Plk_2-3 | 378 | 384 | PF00069 | 0.558 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.643 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.508 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.610 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.458 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.471 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.375 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.703 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.583 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.709 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.792 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.525 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.668 |
TRG_DiLeu_BaEn_2 | 283 | 289 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 372 | 377 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 449 | 454 | PF01217 | 0.664 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.742 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 262 | 265 | PF00400 | 0.662 |
TRG_NES_CRM1_1 | 284 | 297 | PF08389 | 0.687 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2A9 | Leptomonas seymouri | 35% | 96% |
A4HLR1 | Leishmania braziliensis | 68% | 99% |
A4I961 | Leishmania infantum | 98% | 100% |
E9B437 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q3Y8 | Leishmania major | 88% | 99% |