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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A0A3S7WWZ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 896 | 898 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 913 | 915 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 923 | 925 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 929 | 931 | PF00675 | 0.532 |
CLV_PCSK_KEX2_1 | 895 | 897 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 913 | 915 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 923 | 925 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 929 | 931 | PF00082 | 0.532 |
CLV_PCSK_PC7_1 | 892 | 898 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 623 | 627 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 745 | 749 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 806 | 810 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 867 | 871 | PF00082 | 0.521 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 614 | 618 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 797 | 801 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 858 | 862 | PF00917 | 0.529 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.481 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.481 |
LIG_SH3_3 | 925 | 931 | PF00018 | 0.566 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.503 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.484 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.531 |
LIG_TRAF2_1 | 216 | 219 | PF00917 | 0.505 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.482 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.532 |
LIG_TRAF2_1 | 277 | 280 | PF00917 | 0.503 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.480 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.533 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.504 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.532 |
LIG_TRAF2_1 | 399 | 402 | PF00917 | 0.502 |
LIG_TRAF2_1 | 452 | 455 | PF00917 | 0.530 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.506 |
LIG_TRAF2_1 | 513 | 516 | PF00917 | 0.532 |
LIG_TRAF2_1 | 521 | 524 | PF00917 | 0.508 |
LIG_TRAF2_1 | 574 | 577 | PF00917 | 0.521 |
LIG_TRAF2_1 | 582 | 585 | PF00917 | 0.518 |
LIG_TRAF2_1 | 635 | 638 | PF00917 | 0.524 |
LIG_TRAF2_1 | 643 | 646 | PF00917 | 0.515 |
LIG_TRAF2_1 | 696 | 699 | PF00917 | 0.524 |
LIG_TRAF2_1 | 704 | 707 | PF00917 | 0.506 |
LIG_TRAF2_1 | 757 | 760 | PF00917 | 0.521 |
LIG_TRAF2_1 | 765 | 768 | PF00917 | 0.498 |
LIG_TRAF2_1 | 818 | 821 | PF00917 | 0.504 |
LIG_TRAF2_1 | 826 | 829 | PF00917 | 0.491 |
LIG_TRAF2_1 | 86 | 89 | PF00917 | 0.503 |
LIG_TRAF2_1 | 879 | 882 | PF00917 | 0.478 |
LIG_TRAF2_1 | 887 | 890 | PF00917 | 0.431 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.487 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.514 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.545 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.543 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.492 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.544 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.540 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.544 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.543 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.540 |
MOD_CK2_1 | 613 | 619 | PF00069 | 0.548 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.517 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.546 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.548 |
MOD_CK2_1 | 796 | 802 | PF00069 | 0.538 |
MOD_CK2_1 | 857 | 863 | PF00069 | 0.533 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.519 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.550 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.547 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.547 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.544 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.548 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.547 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.544 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.488 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.554 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.521 |
MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.548 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.551 |
MOD_GlcNHglycan | 799 | 802 | PF01048 | 0.543 |
MOD_GlcNHglycan | 860 | 863 | PF01048 | 0.537 |
TRG_ER_diArg_1 | 895 | 897 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 912 | 914 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 923 | 926 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 928 | 930 | PF00400 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4HZS0 | Leishmania infantum | 99% | 100% |