Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_012536595.1 AFE_RS07230 NAD-dependent succinate-semialdehyde dehydrogenase
Query= curated2:Q1QTQ7 (489 letters) >NCBI__GCF_000021485.1:WP_012536595.1 Length = 475 Score = 179 bits (455), Expect = 1e-49 Identities = 148/454 (32%), Positives = 213/454 (46%), Gaps = 23/454 (5%) Query: 9 IDGAWVDGDAARFAKTDPVSGETLWTATAASATQVEHAVAAARQAFPDWARRSFAERQAV 68 IDG W D ARF PV+ + L + + + AV AA AF W + + +R + Sbjct: 10 IDGCWTDL-RARFVVQSPVNQQMLAEVSDCGPREADAAVQAATVAFAAWRQTTVYQRALI 68 Query: 69 VERFRECLETHREHLATAIAQETGKPLWEARTEVGAMIGKVAISITAYHER-----TGER 123 + R+ + ++ H E LA I E GKP+ ++R E+ K A+++ ++ TGE Sbjct: 69 LSRWADLIQVHAEDLARLITWEMGKPIRQSRAEI-----KTAVALARWYAEECKRVTGES 123 Query: 124 -ARDIGDARAVLRHRPHGVLAVYGPYNFPGHLPNGHIVPALLAGNAVVFKPSEQTPMTAD 182 D R + P G + P+N P + I PAL AG V+ KP EQTP++A Sbjct: 124 IPSQFPDKRLQIWKVPIGPVFAITPWNSPVSMVVRKIAPALAAGCTVILKPDEQTPLSAL 183 Query: 183 LTLQCWLEAGLPAGVINLVQGA--AEVGQALAGSADIDGLLFTGSAKVGGLLHRQFGGQV 240 + W A PAG + ++ A A + + L + I L FTGS VG L+ Q G Sbjct: 184 KLAELWAAAEGPAGTLQVLPSADPAPLAERLMADSRIAKLSFTGSTAVGQKLYAQ-GSPT 242 Query: 241 DKILALELGGNNPLVVKDVPDREAAVLSILQSAFASGGQRCTCARRLIVPHGAVGDDLID 300 K L+LELGG+ P+++ D +AAV + + F GQ C A RL V A+ + Sbjct: 243 IKRLSLELGGHAPVLIFADADIDAAVAMTIHAKFRYAGQSCVAANRLYVDE-AILPEFTA 301 Query: 301 ALTSAIAELRVAAPFSEPAPFYAGLTSVEAADGLLAAQDDLVARGGRPL--SRMRRLQAG 358 A+ L+V PF+E L S A A D +ARG R L + L Sbjct: 302 RYLEAMGHLKVGDPFAEDTDI-GPLVSEVAVQKFKAQLQDAMARGARLLCGGDAQGLWCS 360 Query: 359 TSLLSPGLIDVTGCDVPDEEHFGPLLKVHRYRDWDEAIALANDTRYGLSAGLIGGERADW 418 +LL+ +D + EE F PLL + +R EA+A ANDT YGL+A L + Sbjct: 361 PTLLAD--LDPQS-RIFHEESFSPLLPIQGFRSEAEAVARANDTPYGLAAYLWTRDLGRA 417 Query: 419 DDFLLRIRAGIVNWNRQTTGASSDAPFGGIGDSG 452 ++ GIV N A+ APFGG SG Sbjct: 418 YRIAEALQCGIVGVN-DGAPATPQAPFGGSKLSG 450 Lambda K H 0.319 0.135 0.409 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: 33 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: 489 Length of database: 475 Length adjustment: 34 Effective length of query: 455 Effective length of database: 441 Effective search space: 200655 Effective search space used: 200655 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 Apr 09 2024. 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