Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate H281DRAFT_00993 H281DRAFT_00993 gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase
Query= BRENDA::Q4DRT8 (561 letters) >lcl|FitnessBrowser__Burk376:H281DRAFT_00993 H281DRAFT_00993 gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase Length = 497 Score = 150 bits (379), Expect = 1e-40 Identities = 134/440 (30%), Positives = 202/440 (45%), Gaps = 32/440 (7%) Query: 90 KAIDTALQASRE------WSQTSFRDRAAIFLHAAHLISTKYRHELRAATMLGQSKSPFQ 143 K +D A+ A+RE WS+ + R A+ A LI EL L K + Sbjct: 55 KDVDRAVAAAREAFESGVWSKAAPAQRKAVLQRLAQLIDDN-AEELALLEALEAGKPISE 113 Query: 144 AEIDVIAESCDFLRFSVHYAENLYRDQPLSPSSGAVWNSLDYRPLEGFVSTIAPFNFAAI 203 I ES +R+ + Y LSPS +V + + P+ G V + P+NF A+ Sbjct: 114 CLGLDIPESAACIRWHAEVTDKRY--DALSPSGASVVSMITREPI-GVVGAVLPWNFPAL 170 Query: 204 AANLVACPAL-MGNVVLWKPSPHAVLSNYLLYKVFEEAGLPAGVVNFLPCEPDVMTNFVN 262 PAL +GN V+ KP+ LS + + EAGLPAGV+N + + + Sbjct: 171 MLAWKIGPALSVGNSVIVKPAEQTSLSTLRIADLALEAGLPAGVLNVVTGFGESAGQALG 230 Query: 263 SHRDLAGVAFTGSTKVFMSINKQIYARLEEYRNIPRISGETGGKDFHLVHPS-ADLKLAA 321 H D+ VAFTGST+ + + R N+ R+ E GGK+ +V P A+L A Sbjct: 231 RHADVDLVAFTGSTE-----TGKRFLRYSADTNLKRVVLECGGKNPQVVLPDVANLDAVA 285 Query: 322 ALTVRGAFEFQGQKCSATSRLYAPKSRWEELKNYMLGVHEQLKMGQPDDFKSFMCAVIDE 381 V AF G+ CSA SR+ P S L +L V E K G P D + ++I+E Sbjct: 286 EQAVAAAFWNMGENCSAGSRILVPSSLKASLLEKVLAVLEVWKTGDPLDPDVKLGSLIEE 345 Query: 382 TAFERNKKYIDIAKSSPSTYSVIAGGGYDKTE--GWFVQPTIVESKDSQAQLMHEEIFGP 439 FE+ +I+ A++ + ++ GG +T+ GWFV+PTI ++ Q ++ +E+FGP Sbjct: 346 MHFEKVLAHIEKARAEGA--RLVCGGKATRTDSGGWFVEPTIFDNVTPQMRIARDEVFGP 403 Query: 440 ILTVHVYDDSKPGFWSDVCDVVNRSTKYALTGSIFAQDRQAIRDATTKHLRYAAGNYYIN 499 ++ Y D D + T Y L S++ + + A R AG +N Sbjct: 404 VVCFIEYAD------IDEAVHIANDTCYGLAASLWTDN---VNHAHKIAARIRAGTVTVN 454 Query: 500 DKCTGAVVGQQPFGGARASG 519 C G PFGG + SG Sbjct: 455 --CFGEGDLSTPFGGFKQSG 472 Lambda K H 0.320 0.133 0.402 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 591 Number of extensions: 29 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 561 Length of database: 497 Length adjustment: 35 Effective length of query: 526 Effective length of database: 462 Effective search space: 243012 Effective search space used: 243012 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory