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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3Q8IM81
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 9 |
GO:0032259 | methylation | 2 | 9 |
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 | 10 |
GO:0008168 | methyltransferase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.623 |
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.440 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.404 |
CLV_C14_Caspase3-7 | 506 | 510 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 520 | 524 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 525 | 529 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.842 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 633 | 635 | PF00675 | 0.465 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.815 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.819 |
CLV_PCSK_PC7_1 | 170 | 176 | PF00082 | 0.778 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.754 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.541 |
DEG_ODPH_VHL_1 | 425 | 437 | PF01847 | 0.453 |
DEG_SPOP_SBC_1 | 258 | 262 | PF00917 | 0.448 |
DEG_SPOP_SBC_1 | 34 | 38 | PF00917 | 0.541 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.525 |
DOC_CKS1_1 | 556 | 561 | PF01111 | 0.381 |
DOC_MAPK_DCC_7 | 421 | 430 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 284 | 294 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 574 | 582 | PF00069 | 0.344 |
DOC_PP1_RVXF_1 | 288 | 295 | PF00149 | 0.440 |
DOC_PP1_RVXF_1 | 558 | 564 | PF00149 | 0.406 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.293 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.432 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 103 | 107 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 114 | 122 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 160 | 169 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 175 | 185 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 212 | 220 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 299 | 306 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 502 | 508 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 592 | 602 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 633 | 637 | PF00244 | 0.664 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.563 |
LIG_BRCT_BRCA1_1 | 603 | 607 | PF00533 | 0.633 |
LIG_deltaCOP1_diTrp_1 | 462 | 469 | PF00928 | 0.333 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.305 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.467 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.399 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.398 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.272 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.498 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.379 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.637 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.546 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.554 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.375 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.344 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.459 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.609 |
LIG_LIR_Apic_2 | 127 | 132 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 189 | 198 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 273 | 283 | PF02991 | 0.220 |
LIG_LIR_Gen_1 | 462 | 470 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 542 | 552 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 604 | 614 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 622 | 630 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 604 | 610 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 622 | 626 | PF02991 | 0.621 |
LIG_LYPXL_SIV_4 | 117 | 125 | PF13949 | 0.451 |
LIG_REV1ctd_RIR_1 | 291 | 300 | PF16727 | 0.457 |
LIG_REV1ctd_RIR_1 | 412 | 421 | PF16727 | 0.379 |
LIG_SH2_CRK | 544 | 548 | PF00017 | 0.335 |
LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 544 | 548 | PF00017 | 0.335 |
LIG_SH2_SRC | 118 | 121 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 544 | 548 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 220 | 223 | PF00017 | 0.366 |
LIG_SH2_STAT3 | 498 | 501 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.440 |
LIG_SH3_1 | 421 | 427 | PF00018 | 0.461 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.582 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.601 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.387 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.461 |
LIG_SUMO_SIM_par_1 | 403 | 409 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 577 | 584 | PF11976 | 0.344 |
LIG_SxIP_EBH_1 | 549 | 562 | PF03271 | 0.357 |
LIG_TRAF2_1 | 490 | 493 | PF00917 | 0.432 |
LIG_TRAF2_1 | 613 | 616 | PF00917 | 0.628 |
LIG_WW_1 | 92 | 95 | PF00397 | 0.434 |
MOD_CDK_SPK_2 | 555 | 560 | PF00069 | 0.385 |
MOD_CDK_SPxK_1 | 311 | 317 | PF00069 | 0.464 |
MOD_CDK_SPxxK_3 | 555 | 562 | PF00069 | 0.381 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.513 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.515 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.407 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.488 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.556 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.390 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.565 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.607 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.540 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.575 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.481 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.368 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.438 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.588 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.495 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.620 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.495 |
MOD_DYRK1A_RPxSP_1 | 311 | 315 | PF00069 | 0.324 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.663 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.690 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.772 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.729 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.626 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.678 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.610 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.801 |
MOD_GlcNHglycan | 523 | 527 | PF01048 | 0.726 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.457 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.435 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.658 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.702 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.767 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.544 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.549 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.518 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.477 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.496 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.446 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.385 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.522 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.550 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.279 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.367 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.610 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.640 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.518 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.559 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.702 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.587 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.600 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.393 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.404 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.308 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.423 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.219 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.603 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.582 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.501 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.586 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.488 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.539 |
MOD_PIKK_1 | 583 | 589 | PF00454 | 0.607 |
MOD_PKA_1 | 175 | 181 | PF00069 | 0.546 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.473 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.300 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.622 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.536 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.622 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.637 |
MOD_PKB_1 | 500 | 508 | PF00069 | 0.490 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.391 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.501 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.437 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.470 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.528 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.417 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.487 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.352 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.556 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.422 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.538 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.525 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.620 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.462 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.541 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.514 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.383 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.654 |
MOD_SUMO_rev_2 | 94 | 101 | PF00179 | 0.471 |
TRG_DiLeu_BaEn_1 | 305 | 310 | PF01217 | 0.409 |
TRG_DiLeu_BaEn_1 | 575 | 580 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_2 | 270 | 276 | PF01217 | 0.224 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 495 | 498 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 559 | 562 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 589 | 592 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 632 | 634 | PF00400 | 0.675 |
TRG_NLS_MonoExtC_3 | 174 | 180 | PF00514 | 0.633 |
TRG_NLS_MonoExtN_4 | 174 | 179 | PF00514 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 290 | 295 | PF00026 | 0.646 |
TRG_Pf-PMV_PEXEL_1 | 354 | 358 | PF00026 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHP2 | Leptomonas seymouri | 47% | 100% |
A0A1X0NWU4 | Trypanosomatidae | 29% | 100% |
A4HCX9 | Leishmania braziliensis | 74% | 98% |
A4I0G2 | Leishmania infantum | 99% | 100% |
C9ZV78 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AWC5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QB47 | Leishmania major | 89% | 100% |
V5BEP9 | Trypanosoma cruzi | 30% | 100% |