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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0035371 | microtubule plus-end | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990752 | microtubule end | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IEJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097435 | supramolecular fiber organization | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008017 | microtubule binding | 5 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0051010 | microtubule plus-end binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 646 | 650 | PF00656 | 0.639 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.682 |
CLV_PCSK_PC1ET2_1 | 318 | 320 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.418 |
DEG_SCF_FBW7_1 | 658 | 665 | PF00400 | 0.690 |
DOC_CKS1_1 | 659 | 664 | PF01111 | 0.770 |
DOC_CYCLIN_RxL_1 | 480 | 490 | PF00134 | 0.697 |
DOC_CYCLIN_RxL_1 | 636 | 649 | PF00134 | 0.596 |
DOC_CYCLIN_yCln2_LP_2 | 86 | 92 | PF00134 | 0.566 |
DOC_MAPK_gen_1 | 279 | 288 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 32 | 39 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 594 | 603 | PF00069 | 0.619 |
DOC_MAPK_gen_1 | 623 | 632 | PF00069 | 0.776 |
DOC_MAPK_MEF2A_6 | 165 | 172 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 463 | 470 | PF00069 | 0.613 |
DOC_MAPK_MEF2A_6 | 626 | 634 | PF00069 | 0.694 |
DOC_MAPK_RevD_3 | 21 | 34 | PF00069 | 0.634 |
DOC_PP1_RVXF_1 | 174 | 180 | PF00149 | 0.528 |
DOC_PP1_RVXF_1 | 639 | 646 | PF00149 | 0.627 |
DOC_PP1_SILK_1 | 34 | 39 | PF00149 | 0.513 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.533 |
DOC_PP4_FxxP_1 | 579 | 582 | PF00568 | 0.518 |
DOC_PP4_FxxP_1 | 659 | 662 | PF00568 | 0.739 |
DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.716 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.686 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.736 |
LIG_14-3-3_CanoR_1 | 523 | 527 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 594 | 599 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 609 | 618 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.641 |
LIG_Actin_WH2_2 | 130 | 147 | PF00022 | 0.642 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.706 |
LIG_DLG_GKlike_1 | 594 | 601 | PF00625 | 0.658 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.679 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.495 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.625 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.545 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.550 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.588 |
LIG_LIR_Apic_2 | 612 | 618 | PF02991 | 0.684 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.420 |
LIG_NRBOX | 373 | 379 | PF00104 | 0.562 |
LIG_NRBOX | 597 | 603 | PF00104 | 0.657 |
LIG_RPA_C_Fungi | 213 | 225 | PF08784 | 0.691 |
LIG_SH2_SRC | 90 | 93 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 591 | 595 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.353 |
LIG_SH3_2 | 89 | 94 | PF14604 | 0.494 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.693 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.364 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 18 | 25 | PF11976 | 0.505 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.571 |
LIG_TRAF2_1 | 417 | 420 | PF00917 | 0.582 |
LIG_WRC_WIRS_1 | 17 | 22 | PF05994 | 0.509 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.605 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.537 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.796 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.516 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.646 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.481 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.584 |
MOD_Cter_Amidation | 546 | 549 | PF01082 | 0.451 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.668 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.647 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.359 |
MOD_GlcNHglycan | 266 | 270 | PF01048 | 0.692 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.610 |
MOD_GlcNHglycan | 566 | 570 | PF01048 | 0.675 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.737 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.592 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.754 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.575 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.592 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.774 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.775 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.573 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.711 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.681 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.607 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.538 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.552 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.374 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.566 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.748 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.553 |
MOD_PIKK_1 | 617 | 623 | PF00454 | 0.610 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.740 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.705 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.729 |
MOD_PKA_2 | 625 | 631 | PF00069 | 0.663 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.759 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.542 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.704 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.490 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.480 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.691 |
MOD_Plk_2-3 | 462 | 468 | PF00069 | 0.665 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.516 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.718 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.738 |
MOD_SUMO_for_1 | 104 | 107 | PF00179 | 0.569 |
MOD_SUMO_for_1 | 157 | 160 | PF00179 | 0.698 |
MOD_SUMO_for_1 | 354 | 357 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 160 | 167 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 184 | 193 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 300 | 307 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 379 | 387 | PF00179 | 0.511 |
TRG_DiLeu_BaEn_1 | 373 | 378 | PF01217 | 0.561 |
TRG_DiLeu_BaEn_1 | 420 | 425 | PF01217 | 0.604 |
TRG_DiLeu_BaEn_4 | 369 | 375 | PF01217 | 0.658 |
TRG_DiLeu_BaLyEn_6 | 638 | 643 | PF01217 | 0.738 |
TRG_DiLeu_LyEn_5 | 420 | 425 | PF01217 | 0.506 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 421 | 424 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.709 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.661 |
TRG_Pf-PMV_PEXEL_1 | 596 | 600 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSH8 | Leptomonas seymouri | 37% | 93% |
A4HA45 | Leishmania braziliensis | 69% | 95% |
A4HYB1 | Leishmania infantum | 100% | 100% |
E9AS44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |
Q4QDC2 | Leishmania major | 88% | 98% |