Align Glutarate-semialdehyde dehydrogenase; EC 1.2.1.- (characterized)
to candidate WP_106712838.1 CU102_RS19905 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q9I6M5 (483 letters) >NCBI__GCF_003010955.1:WP_106712838.1 Length = 484 Score = 689 bits (1777), Expect = 0.0 Identities = 326/483 (67%), Positives = 407/483 (84%) Query: 1 MQLKDAKLFRQQAYVDGAWVDADNGQTIKVNNPATGEIIGSVPKMGAAETRRAIEAADKA 60 M LKD+ LFRQ A V G W++A+ + + NPATG+ +G VP++G ETR+AI+ A A Sbjct: 1 MVLKDSTLFRQAALVGGQWIEANPANSNLIRNPATGDKLGYVPELGTLETRQAIDVARVA 60 Query: 61 LPAWRALTAKERANKLRRWFDLMIENQDDLARLMTIEQGKPLAEAKGEIAYAASFLEWFG 120 +W TAKER+N LR WF+L+++++ +LAR++T+EQGKPL EA+GEI Y ASF+EW+ Sbjct: 61 QKSWARQTAKERSNVLRCWFELILQHKQELARILTLEQGKPLLEAEGEIVYGASFIEWYA 120 Query: 121 EEAKRIYGDTIPGHQPDKRIIVIKQPIGVTAAITPWNFPSAMITRKAGPALAAGCTMVLK 180 EEA+R+YGD IPGH DKRI+V+KQPIGV AAITPWNFP+AM+TRKAGPALAAGC +VLK Sbjct: 121 EEARRVYGDIIPGHHKDKRILVMKQPIGVVAAITPWNFPNAMVTRKAGPALAAGCAVVLK 180 Query: 181 PASQTPYSALALAELAERAGIPKGVFSVVTGSAGEVGGELTSNPIVRKLTFTGSTEIGRQ 240 PA QTP+SALALA LAE+AG+P+G+FSV+TGSA E+G E+TSNPIVRKLTFTGST +G + Sbjct: 181 PAPQTPFSALALAVLAEQAGLPEGLFSVITGSAVEIGAEMTSNPIVRKLTFTGSTPVGTE 240 Query: 241 LMAECAQDIKKVSLELGGNAPFIVFDDADLDAAVEGALISKYRNNGQTCVCANRLYVQDG 300 L A IKK+ LELGGNAPFIVFDDAD++AAVEGA+I+K+RNNGQTCVCANR+Y+Q+G Sbjct: 241 LYRRSAGTIKKLGLELGGNAPFIVFDDADVEAAVEGAMIAKFRNNGQTCVCANRMYIQNG 300 Query: 301 VYDAFVDKLKAAVAKLNIGNGLEAGVTTGPLIDAKAVAKVEEHIADAVSKGAKVVSGGKP 360 +YDAF KL A VAKL +GNGLE+ V GPLI+A AV KVE+HI+DA+SKGA+V+SGGK Sbjct: 301 IYDAFGQKLSAKVAKLRVGNGLESNVDLGPLINAAAVQKVEDHISDAISKGARVLSGGKA 360 Query: 361 HALGGTFFEPTILVDVPKNALVSKDETFGPLAPVFRFKDEAEVIAMSNDTEFGLASYFYA 420 H+LGGTFFEPT+L DV L + +ETFGP+AP+FRF DE +V+ +NDTEFGLA+YFY+ Sbjct: 361 HSLGGTFFEPTVLSDVTVGMLFASEETFGPVAPLFRFADEDDVVRQANDTEFGLAAYFYS 420 Query: 421 RDLARVFRVAEQLEYGMVGINTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEIKYLCL 480 DLARVFR+AE LEYGMVG+NTGL+S APFGG+K+SGLGREGSKYGI+D+LEIKY+CL Sbjct: 421 ADLARVFRIAEALEYGMVGVNTGLVSTAEAPFGGVKSSGLGREGSKYGIDDFLEIKYVCL 480 Query: 481 GGI 483 GGI Sbjct: 481 GGI 483 Lambda K H 0.317 0.135 0.391 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: 719 Number of extensions: 18 Number of successful extensions: 1 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: 483 Length of database: 484 Length adjustment: 34 Effective length of query: 449 Effective length of database: 450 Effective search space: 202050 Effective search space used: 202050 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 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:
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