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: E9AGV5
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 | 577 | 581 | PF00656 | 0.329 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.682 |
CLV_PCSK_FUR_1 | 252 | 256 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 707 | 711 | PF00082 | 0.462 |
CLV_Separin_Metazoa | 49 | 53 | PF03568 | 0.332 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.604 |
DEG_APCC_DBOX_1 | 418 | 426 | PF00400 | 0.323 |
DEG_SCF_FBW7_1 | 536 | 541 | PF00400 | 0.527 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.445 |
DEG_SPOP_SBC_1 | 487 | 491 | PF00917 | 0.605 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 41 | PF00134 | 0.355 |
DOC_MAPK_gen_1 | 461 | 469 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 566 | 574 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 646 | 654 | PF00069 | 0.285 |
DOC_PP1_RVXF_1 | 154 | 161 | PF00149 | 0.459 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.433 |
DOC_PP2B_LxvP_1 | 688 | 691 | PF13499 | 0.281 |
DOC_PP4_FxxP_1 | 523 | 526 | PF00568 | 0.552 |
DOC_PP4_MxPP_1 | 514 | 517 | PF00568 | 0.585 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.342 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 657 | 662 | PF00397 | 0.376 |
LIG_14-3-3_CanoR_1 | 122 | 128 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 190 | 200 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 304 | 310 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 449 | 454 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 471 | 481 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 56 | 61 | PF00244 | 0.433 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.401 |
LIG_Actin_WH2_2 | 203 | 221 | PF00022 | 0.415 |
LIG_Actin_WH2_2 | 278 | 293 | PF00022 | 0.394 |
LIG_BIR_III_4 | 163 | 167 | PF00653 | 0.355 |
LIG_BRCT_BRCA1_1 | 156 | 160 | PF00533 | 0.468 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.348 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.421 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.520 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.293 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.454 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.296 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.345 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.447 |
LIG_FHA_1 | 704 | 710 | PF00498 | 0.281 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.534 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.365 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.400 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.620 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.445 |
LIG_FHA_2 | 695 | 701 | PF00498 | 0.281 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.604 |
LIG_LIR_Apic_2 | 521 | 526 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 264 | 274 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 411 | 422 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 593 | 601 | PF02991 | 0.329 |
LIG_LIR_LC3C_4 | 568 | 573 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 589 | 594 | PF02991 | 0.329 |
LIG_PCNA_yPIPBox_3 | 44 | 56 | PF02747 | 0.364 |
LIG_REV1ctd_RIR_1 | 118 | 128 | PF16727 | 0.430 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.367 |
LIG_SH2_CRK | 554 | 558 | PF00017 | 0.281 |
LIG_SH2_PTP2 | 594 | 597 | PF00017 | 0.281 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.762 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 694 | 697 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.436 |
LIG_SH3_1 | 234 | 240 | PF00018 | 0.424 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.536 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.572 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.603 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.650 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.737 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.281 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.296 |
LIG_SH3_3 | 673 | 679 | PF00018 | 0.231 |
LIG_SUMO_SIM_anti_2 | 568 | 574 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 570 | 577 | PF11976 | 0.329 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.340 |
LIG_TRAF2_1 | 565 | 568 | PF00917 | 0.282 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.386 |
LIG_WW_3 | 7 | 11 | PF00397 | 0.721 |
MOD_CDK_SPxxK_3 | 3 | 10 | PF00069 | 0.542 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.420 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.357 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.522 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.386 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.347 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.541 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.688 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.659 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.588 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.242 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.361 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.410 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.464 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.351 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.621 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.434 |
MOD_CK2_1 | 623 | 629 | PF00069 | 0.281 |
MOD_CK2_1 | 694 | 700 | PF00069 | 0.329 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.397 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.449 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.396 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.294 |
MOD_GlcNHglycan | 636 | 640 | PF01048 | 0.327 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.352 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.611 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.483 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.410 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.423 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.483 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.388 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.369 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.351 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.686 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.557 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.557 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.572 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.317 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.323 |
MOD_LATS_1 | 54 | 60 | PF00433 | 0.425 |
MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.401 |
MOD_N-GLC_1 | 670 | 675 | PF02516 | 0.265 |
MOD_N-GLC_2 | 398 | 400 | PF02516 | 0.472 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.478 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.378 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.436 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.560 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.401 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.334 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.329 |
MOD_NEK2_2 | 672 | 677 | PF00069 | 0.259 |
MOD_NEK2_2 | 694 | 699 | PF00069 | 0.329 |
MOD_NEK2_2 | 87 | 92 | PF00069 | 0.451 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.386 |
MOD_PIKK_1 | 470 | 476 | PF00454 | 0.594 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.605 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.441 |
MOD_PK_1 | 455 | 461 | PF00069 | 0.581 |
MOD_PKA_1 | 383 | 389 | PF00069 | 0.340 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.652 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.397 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.571 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.319 |
MOD_PKB_1 | 255 | 263 | PF00069 | 0.473 |
MOD_PKB_1 | 309 | 317 | PF00069 | 0.375 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.524 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.411 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.359 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.482 |
MOD_Plk_1 | 670 | 676 | PF00069 | 0.265 |
MOD_Plk_1 | 707 | 713 | PF00069 | 0.479 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.451 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.482 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.347 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.511 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.446 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.556 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.560 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.575 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.259 |
MOD_ProDKin_1 | 657 | 663 | PF00069 | 0.376 |
MOD_SUMO_for_1 | 565 | 568 | PF00179 | 0.329 |
TRG_DiLeu_BaEn_1 | 423 | 428 | PF01217 | 0.382 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.415 |
TRG_DiLeu_BaEn_1 | 700 | 705 | PF01217 | 0.329 |
TRG_DiLeu_LyEn_5 | 53 | 58 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.281 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 338 | 341 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 470 | 472 | PF00400 | 0.688 |
TRG_NES_CRM1_1 | 13 | 27 | PF08389 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 26 | 31 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 449 | 453 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P826 | Leptomonas seymouri | 47% | 100% |
A0A3Q8IF57 | Leishmania donovani | 99% | 100% |
Q4QCB0 | Leishmania major | 92% | 100% |