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: A4HCX9
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 | 323 | 327 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.422 |
CLV_C14_Caspase3-7 | 433 | 437 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.557 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.459 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.834 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.834 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.769 |
CLV_Separin_Metazoa | 462 | 466 | PF03568 | 0.390 |
DEG_ODPH_VHL_1 | 410 | 422 | PF01847 | 0.434 |
DOC_CKS1_1 | 298 | 303 | PF01111 | 0.398 |
DOC_CKS1_1 | 541 | 546 | PF01111 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.420 |
DOC_MAPK_DCC_7 | 406 | 415 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 270 | 280 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 370 | 378 | PF00069 | 0.301 |
DOC_MAPK_gen_1 | 442 | 451 | PF00069 | 0.246 |
DOC_MAPK_MEF2A_6 | 445 | 453 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 559 | 567 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 274 | 281 | PF00149 | 0.445 |
DOC_PP1_RVXF_1 | 443 | 449 | PF00149 | 0.238 |
DOC_PP1_RVXF_1 | 543 | 549 | PF00149 | 0.401 |
DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.578 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.282 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.540 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 104 | 108 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 114 | 123 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 162 | 172 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 285 | 292 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 349 | 353 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 465 | 473 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 618 | 622 | PF00244 | 0.657 |
LIG_APCC_ABBA_1 | 252 | 257 | PF00400 | 0.310 |
LIG_BIR_III_2 | 308 | 312 | PF00653 | 0.409 |
LIG_BIR_III_4 | 650 | 654 | PF00653 | 0.658 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.362 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 588 | 592 | PF00533 | 0.619 |
LIG_deltaCOP1_diTrp_1 | 447 | 454 | PF00928 | 0.321 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.573 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.560 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.382 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.628 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.418 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.627 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.486 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.438 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.363 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.409 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.326 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.424 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.606 |
LIG_LIR_Apic_2 | 128 | 133 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 345 | 352 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 447 | 454 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 527 | 537 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 589 | 599 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 607 | 615 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 260 | 264 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 607 | 611 | PF02991 | 0.589 |
LIG_LYPXL_SIV_4 | 118 | 126 | PF13949 | 0.444 |
LIG_OCRL_FandH_1 | 278 | 290 | PF00620 | 0.275 |
LIG_PCNA_yPIPBox_3 | 480 | 493 | PF02747 | 0.326 |
LIG_REV1ctd_RIR_1 | 277 | 286 | PF16727 | 0.460 |
LIG_REV1ctd_RIR_1 | 397 | 406 | PF16727 | 0.367 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.275 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.338 |
LIG_SH2_GRB2like | 130 | 133 | PF00017 | 0.519 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.275 |
LIG_SH2_NCK_1 | 529 | 533 | PF00017 | 0.325 |
LIG_SH2_SRC | 119 | 122 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 529 | 533 | PF00017 | 0.338 |
LIG_SH2_STAT3 | 207 | 210 | PF00017 | 0.373 |
LIG_SH2_STAT3 | 483 | 486 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.454 |
LIG_SH3_1 | 406 | 412 | PF00018 | 0.461 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.467 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.566 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.470 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.413 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.464 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.396 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.461 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.474 |
LIG_SH3_CIN85_PxpxPR_1 | 2 | 7 | PF14604 | 0.435 |
LIG_Sin3_3 | 534 | 541 | PF02671 | 0.231 |
LIG_SUMO_SIM_par_1 | 562 | 569 | PF11976 | 0.335 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.297 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.410 |
LIG_WW_3 | 300 | 304 | PF00397 | 0.329 |
MOD_CDK_SPK_2 | 540 | 545 | PF00069 | 0.390 |
MOD_CDK_SPxK_1 | 297 | 303 | PF00069 | 0.457 |
MOD_CDK_SPxxK_3 | 540 | 547 | PF00069 | 0.385 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.544 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.523 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.408 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.548 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.514 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.426 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.582 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.598 |
MOD_CK1_1 | 633 | 639 | PF00069 | 0.547 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.468 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.526 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.564 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.328 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.437 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.449 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.361 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.542 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.229 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.580 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.456 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.478 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.656 |
MOD_DYRK1A_RPxSP_1 | 297 | 301 | PF00069 | 0.317 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.677 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.644 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.746 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.705 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.755 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.746 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.615 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.658 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.769 |
MOD_GlcNHglycan | 508 | 512 | PF01048 | 0.745 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.431 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.431 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.663 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.717 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.738 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.785 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.562 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.532 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.555 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.579 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.469 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.502 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.426 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.450 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.526 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.558 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.293 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.391 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.631 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.503 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.557 |
MOD_LATS_1 | 283 | 289 | PF00433 | 0.321 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.739 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.600 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.730 |
MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.679 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.533 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.309 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.417 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.216 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.384 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.640 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.519 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.536 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.431 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.527 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.374 |
MOD_PIKK_1 | 568 | 574 | PF00454 | 0.582 |
MOD_PKA_1 | 114 | 120 | PF00069 | 0.275 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.467 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.455 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.626 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.403 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.323 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.433 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.475 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.633 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.649 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.332 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.508 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.444 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.365 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.450 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.479 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.411 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.533 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.474 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.339 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.586 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.543 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.615 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.461 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.508 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.387 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.644 |
MOD_SUMO_rev_2 | 165 | 175 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 94 | 102 | PF00179 | 0.443 |
TRG_DiLeu_BaEn_1 | 291 | 296 | PF01217 | 0.416 |
TRG_DiLeu_BaEn_1 | 560 | 565 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.338 |
TRG_ER_diArg_1 | 103 | 105 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.293 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 480 | 483 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 544 | 547 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 617 | 619 | PF00400 | 0.664 |
TRG_NES_CRM1_1 | 340 | 354 | PF08389 | 0.277 |
TRG_Pf-PMV_PEXEL_1 | 276 | 281 | PF00026 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.647 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHP2 | Leptomonas seymouri | 47% | 100% |
A0A1X0NWU4 | Trypanosomatidae | 30% | 100% |
A0A3Q8IM81 | Leishmania donovani | 74% | 98% |
A0A3R7NJ73 | Trypanosoma rangeli | 32% | 100% |
A4I0G2 | Leishmania infantum | 74% | 98% |
C9ZV78 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AWC5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 98% |
Q4QB47 | Leishmania major | 73% | 100% |
V5BEP9 | Trypanosoma cruzi | 31% | 100% |