Homologous to S-adenosylmethionine sensor upstream of mTORC1. Does not appear to be membrane-associated.
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AWC5
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 10 |
GO:0032259 | methylation | 2 | 10 |
GO:0009966 | regulation of signal transduction | 4 | 1 |
GO:0009968 | negative regulation of signal transduction | 5 | 1 |
GO:0010646 | regulation of cell communication | 4 | 1 |
GO:0010648 | negative regulation of cell communication | 5 | 1 |
GO:0023051 | regulation of signaling | 3 | 1 |
GO:0023057 | negative regulation of signaling | 4 | 1 |
GO:0032006 | regulation of TOR signaling | 6 | 1 |
GO:0032007 | negative regulation of TOR signaling | 7 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0048585 | negative regulation of response to stimulus | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
GO:1902532 | negative regulation of intracellular signal transduction | 6 | 1 |
GO:1903432 | regulation of TORC1 signaling | 7 | 1 |
GO:1904262 | negative regulation of TORC1 signaling | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 506 | 510 | PF00656 | 0.569 |
CLV_C14_Caspase3-7 | 520 | 524 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 633 | 635 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.826 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.826 |
CLV_PCSK_PC7_1 | 170 | 176 | PF00082 | 0.770 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.410 |
DEG_ODPH_VHL_1 | 323 | 336 | PF01847 | 0.348 |
DEG_ODPH_VHL_1 | 425 | 437 | PF01847 | 0.451 |
DEG_SPOP_SBC_1 | 258 | 262 | PF00917 | 0.404 |
DOC_CKS1_1 | 312 | 317 | PF01111 | 0.434 |
DOC_CKS1_1 | 556 | 561 | PF01111 | 0.376 |
DOC_MAPK_DCC_7 | 421 | 430 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 284 | 294 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 574 | 582 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 288 | 295 | PF00149 | 0.435 |
DOC_PP1_RVXF_1 | 558 | 564 | PF00149 | 0.396 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.357 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.616 |
LIG_14-3-3_CanoR_1 | 103 | 107 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 114 | 122 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 175 | 185 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 212 | 220 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 299 | 306 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 592 | 602 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 633 | 637 | PF00244 | 0.649 |
LIG_APCC_ABBA_1 | 266 | 271 | PF00400 | 0.311 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.563 |
LIG_BRCT_BRCA1_1 | 603 | 607 | PF00533 | 0.622 |
LIG_deltaCOP1_diTrp_1 | 462 | 469 | PF00928 | 0.327 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.605 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.417 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.385 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.502 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.375 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.624 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.409 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.488 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.359 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.324 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.342 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.414 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.603 |
LIG_Integrin_RGD_1 | 460 | 462 | PF01839 | 0.433 |
LIG_Integrin_RGDW_4 | 460 | 463 | PF00362 | 0.426 |
LIG_LIR_Apic_2 | 127 | 132 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 462 | 470 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 542 | 552 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 604 | 614 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 622 | 630 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 635 | 644 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 332 | 336 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 604 | 610 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 622 | 626 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 635 | 639 | PF02991 | 0.559 |
LIG_LYPXL_SIV_4 | 117 | 125 | PF13949 | 0.458 |
LIG_REV1ctd_RIR_1 | 291 | 300 | PF16727 | 0.427 |
LIG_REV1ctd_RIR_1 | 412 | 421 | PF16727 | 0.396 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.340 |
LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.506 |
LIG_SH2_NCK_1 | 544 | 548 | PF00017 | 0.340 |
LIG_SH2_SRC | 118 | 121 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 386 | 390 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 544 | 548 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 220 | 223 | PF00017 | 0.405 |
LIG_SH2_STAT3 | 269 | 272 | PF00017 | 0.264 |
LIG_SH2_STAT3 | 498 | 501 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.334 |
LIG_SH3_1 | 421 | 427 | PF00018 | 0.460 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.560 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.591 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.408 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.462 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.460 |
LIG_SUMO_SIM_par_1 | 403 | 409 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 577 | 584 | PF11976 | 0.335 |
LIG_SxIP_EBH_1 | 549 | 562 | PF03271 | 0.346 |
LIG_TRAF2_1 | 490 | 493 | PF00917 | 0.422 |
LIG_TRAF2_1 | 613 | 616 | PF00917 | 0.625 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.428 |
LIG_WW_1 | 92 | 95 | PF00397 | 0.438 |
MOD_CDK_SPK_2 | 555 | 560 | PF00069 | 0.380 |
MOD_CDK_SPxxK_3 | 555 | 562 | PF00069 | 0.377 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.443 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.629 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.540 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.409 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.493 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.406 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.508 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.500 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.571 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.524 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.577 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.591 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.547 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.491 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.350 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.524 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.581 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.440 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.588 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.481 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.673 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.672 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.747 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.664 |
MOD_GlcNHglycan | 341 | 345 | PF01048 | 0.715 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.636 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.700 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.631 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.640 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.769 |
MOD_GlcNHglycan | 523 | 527 | PF01048 | 0.717 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.419 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.425 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.676 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.748 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.415 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.505 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.568 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.467 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.490 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.434 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.467 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.462 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.553 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.454 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.332 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.537 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.278 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.371 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.627 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.512 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.568 |
MOD_N-GLC_2 | 311 | 313 | PF02516 | 0.457 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.551 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.472 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.298 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.419 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.207 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.627 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.511 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.493 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.527 |
MOD_PIKK_1 | 583 | 589 | PF00454 | 0.571 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.482 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.347 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.620 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.412 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.625 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.644 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.393 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.398 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.468 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.447 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.472 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.600 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.415 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.488 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.330 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.604 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.608 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.489 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.426 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.536 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.466 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.405 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.379 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.620 |
MOD_SUMO_rev_2 | 94 | 101 | PF00179 | 0.478 |
TRG_DiLeu_BaEn_1 | 305 | 310 | PF01217 | 0.416 |
TRG_DiLeu_BaEn_1 | 575 | 580 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 495 | 498 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 559 | 562 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 632 | 634 | PF00400 | 0.657 |
TRG_NLS_MonoExtN_4 | 325 | 330 | PF00514 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 104 | 109 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 290 | 295 | PF00026 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 354 | 358 | PF00026 | 0.648 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.614 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHP2 | Leptomonas seymouri | 49% | 100% |
A0A1X0NWU4 | Trypanosomatidae | 29% | 100% |
A0A3Q8IM81 | Leishmania donovani | 87% | 100% |
A0A3R7NJ73 | Trypanosoma rangeli | 29% | 100% |
A4HCX9 | Leishmania braziliensis | 73% | 98% |
A4I0G2 | Leishmania infantum | 87% | 100% |
C9ZV78 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
Q4QB47 | Leishmania major | 85% | 100% |
V5BEP9 | Trypanosoma cruzi | 28% | 100% |