Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_053939191.1 WG78_RS17855 trifunctional transcriptional regulator/proline dehydrogenase/L-glutamate gamma-semialdehyde dehydrogenase
Query= curated2:Q87L22 (485 letters) >NCBI__GCF_001294205.1:WP_053939191.1 Length = 1316 Score = 180 bits (456), Expect = 3e-49 Identities = 143/464 (30%), Positives = 229/464 (49%), Gaps = 36/464 (7%) Query: 4 WIAGEWVQGQGEEFVSLSPYN-QEVIWRGNGATAEQVDQAVAAARAAFVEWKKRPFAERE 62 W+A GE+ +P + ++V+ A + V A+ A+ A W+ P R Sbjct: 640 WLATPPHAAAGEKQAVRNPADHRDVVGYVVEAALDDVAAALTRAQNAGPIWQATPAVTRA 699 Query: 63 AIVLAFAEKVKENSEKIAEVIAKETGKPIWETRTEAAAMAGKIAISIRAYHDRTGEATRE 122 A++ A+ ++ + + +I +E GK T + A A + +R Y + Sbjct: 700 ALLERAADLMEAEMQTLMGLIVREAGK----TLSNAIAEVREAVDFLRYY-------AAQ 748 Query: 123 AAGNQIVLRHRPLGVMAVFGPYNFPGHLPNGHIVPALLAGNTVVFKPSEQTPWTGELAMK 182 G+ HRPLG + P+NFP + G + AL AGNTV+ KP+EQTP A++ Sbjct: 749 VRGSFSNDTHRPLGPVVCISPWNFPLAIFTGQVAAALAAGNTVLAKPAEQTPLIAAQAVR 808 Query: 183 LWEEAGLPKGVINLVQGAKET-GIALADAKGIDGILFTGSANTGHILHRQFA------GQ 235 + EAG+P+ + L+ G ET G AL + G++FTGS IL R A GQ Sbjct: 809 ILHEAGVPQDAVQLLPGQGETVGAALVGDARVKGVMFTGSTEVARILQRNLAGRLDAHGQ 868 Query: 236 PGKMLALEMGGNNPMVISDNYGDLDATVYTIIQSAFISAGQRCTCARRLYVPFGEKGDAL 295 P ++A E GG N M++ D+ + V ++ SAF SAGQRC+ R L + + D + Sbjct: 869 PIPLIA-ETGGQNAMIV-DSSALAEQVVGDVLASAFDSAGQRCSALRVLCLQ-EDVADRV 925 Query: 296 ITKLVEATKNIRMDQPFAEPAPFMGPQISVAAAKFILDAQANLQSLGGESLIEAKAGEA- 354 +T L + + P A +GP I A + I ++ + G + + + G A Sbjct: 926 LTMLKGGLAELVVGNP-DRLATDVGPVIDAEAQRNI-NSHIDAMRARGRKVHQVQTGAAC 983 Query: 355 ---AFVSPGIIDVTNIAELPDEEYFGPLLQVVRYE------GLDKAVELANDTRFGLSAG 405 +FV P +I++ ++AEL + E FGP+L VVR++ GLD ++ N T +GL+ G Sbjct: 984 NQGSFVPPTLIELDSLAEL-EREIFGPVLHVVRWQRTADQAGLDALIDDINGTGYGLTLG 1042 Query: 406 LVSTDDQEWEYFVDHIRAGIVNRNRQLTGA-SGDAPFGGPGASG 448 + + D+ + V+ + G + NR + GA G PFGG G SG Sbjct: 1043 IHTRIDETIAHIVERAQVGNLYVNRNIVGAVVGVQPFGGEGLSG 1086 Lambda K H 0.316 0.134 0.397 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: 1448 Number of extensions: 89 Number of successful extensions: 8 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: 485 Length of database: 1316 Length adjustment: 41 Effective length of query: 444 Effective length of database: 1275 Effective search space: 566100 Effective search space used: 566100 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 (21.6 bits) S2: 55 (25.8 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