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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IF57
Term | Name | Level | Count |
---|---|---|---|
GO:0007015 | actin filament organization | 5 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016043 | cellular component organization | 3 | 5 |
GO:0071840 | cellular component organization or biogenesis | 2 | 5 |
GO:0097435 | supramolecular fiber organization | 4 | 5 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0019932 | second-messenger-mediated signaling | 4 | 1 |
GO:0019933 | cAMP-mediated signaling | 6 | 1 |
GO:0019935 | cyclic-nucleotide-mediated signaling | 5 | 1 |
GO:0031279 | regulation of cyclase activity | 4 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0045761 | regulation of adenylate cyclase activity | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051339 | regulation of lyase activity | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0005515 | protein binding | 2 | 5 |
GO:0008092 | cytoskeletal protein binding | 3 | 5 |
GO:0008179 | adenylate cyclase binding | 4 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 574 | 578 | PF00656 | 0.323 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.201 |
CLV_PCSK_FUR_1 | 249 | 253 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.201 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 704 | 708 | PF00082 | 0.484 |
CLV_Separin_Metazoa | 49 | 53 | PF03568 | 0.332 |
DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.445 |
DEG_APCC_DBOX_1 | 415 | 423 | PF00400 | 0.336 |
DEG_SCF_FBW7_1 | 533 | 538 | PF00400 | 0.503 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.500 |
DEG_SPOP_SBC_1 | 484 | 488 | PF00917 | 0.629 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.569 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 41 | PF00134 | 0.383 |
DOC_MAPK_gen_1 | 458 | 466 | PF00069 | 0.642 |
DOC_MAPK_MEF2A_6 | 563 | 571 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 643 | 651 | PF00069 | 0.282 |
DOC_PP1_RVXF_1 | 151 | 158 | PF00149 | 0.501 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.464 |
DOC_PP2B_LxvP_1 | 685 | 688 | PF13499 | 0.278 |
DOC_PP4_FxxP_1 | 520 | 523 | PF00568 | 0.578 |
DOC_PP4_MxPP_1 | 511 | 514 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.255 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.255 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.255 |
LIG_14-3-3_CanoR_1 | 119 | 125 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 187 | 197 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 446 | 451 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 468 | 478 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 56 | 61 | PF00244 | 0.452 |
LIG_Actin_WH2_2 | 200 | 218 | PF00022 | 0.439 |
LIG_Actin_WH2_2 | 275 | 290 | PF00022 | 0.395 |
LIG_BIR_III_4 | 160 | 164 | PF00653 | 0.385 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.519 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.353 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.326 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.278 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.323 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.291 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.303 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.278 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.278 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.421 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.369 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.414 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.630 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.449 |
LIG_FHA_2 | 692 | 698 | PF00498 | 0.278 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.506 |
LIG_LIR_Apic_2 | 518 | 523 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 261 | 271 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 408 | 419 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 590 | 598 | PF02991 | 0.323 |
LIG_LIR_LC3C_4 | 565 | 570 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 586 | 591 | PF02991 | 0.323 |
LIG_PCNA_yPIPBox_3 | 44 | 56 | PF02747 | 0.363 |
LIG_REV1ctd_RIR_1 | 115 | 125 | PF16727 | 0.484 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.411 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.278 |
LIG_SH2_PTP2 | 591 | 594 | PF00017 | 0.278 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 691 | 694 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.439 |
LIG_SH3_1 | 231 | 237 | PF00018 | 0.444 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.444 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.614 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.597 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.649 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.638 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.278 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.278 |
LIG_SUMO_SIM_anti_2 | 565 | 571 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 567 | 574 | PF11976 | 0.323 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.339 |
LIG_TRAF2_1 | 562 | 565 | PF00917 | 0.279 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.392 |
LIG_WW_3 | 7 | 11 | PF00397 | 0.635 |
MOD_CDK_SPxxK_3 | 3 | 10 | PF00069 | 0.571 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.466 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.369 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.562 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.394 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.354 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.581 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.605 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.595 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.508 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.362 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.305 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.453 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.475 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.366 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.629 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.441 |
MOD_CK2_1 | 620 | 626 | PF00069 | 0.278 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.323 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.377 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.423 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.359 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.487 |
MOD_GlcNHglycan | 633 | 637 | PF01048 | 0.278 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.278 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.633 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.544 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.461 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.287 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.524 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.458 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.356 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.666 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.473 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.449 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.430 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.262 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.278 |
MOD_LATS_1 | 54 | 60 | PF00433 | 0.439 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.435 |
MOD_N-GLC_1 | 667 | 672 | PF02516 | 0.282 |
MOD_N-GLC_2 | 395 | 397 | PF02516 | 0.494 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.525 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.212 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.423 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.596 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.400 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.323 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.189 |
MOD_NEK2_2 | 669 | 674 | PF00069 | 0.255 |
MOD_NEK2_2 | 691 | 696 | PF00069 | 0.323 |
MOD_NEK2_2 | 87 | 92 | PF00069 | 0.460 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.424 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.560 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.633 |
MOD_PIKK_1 | 540 | 546 | PF00454 | 0.449 |
MOD_PK_1 | 452 | 458 | PF00069 | 0.630 |
MOD_PKA_1 | 380 | 386 | PF00069 | 0.348 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.693 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.471 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.562 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.278 |
MOD_PKB_1 | 252 | 260 | PF00069 | 0.510 |
MOD_PKB_1 | 306 | 314 | PF00069 | 0.387 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.554 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.400 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.473 |
MOD_Plk_1 | 667 | 673 | PF00069 | 0.282 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.508 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.428 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.480 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.354 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.441 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.323 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.592 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.564 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.521 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.255 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.255 |
MOD_SUMO_for_1 | 562 | 565 | PF00179 | 0.323 |
TRG_DiLeu_BaEn_1 | 420 | 425 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.410 |
TRG_DiLeu_BaEn_1 | 697 | 702 | PF01217 | 0.323 |
TRG_DiLeu_LyEn_5 | 53 | 58 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 591 | 594 | PF00928 | 0.278 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 467 | 469 | PF00400 | 0.661 |
TRG_NES_CRM1_1 | 13 | 27 | PF08389 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.557 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P826 | Leptomonas seymouri | 47% | 100% |
E9AGV5 | Leishmania infantum | 99% | 100% |
Q4QCB0 | Leishmania major | 91% | 100% |