Align succinate-semialdehyde dehydrogenase (NADP+) [EC: 1.2.1.16] (characterized)
to candidate WP_038021191.1 HA49_RS06075 NAD-dependent succinate-semialdehyde dehydrogenase
Query= reanno::MR1:200453 (482 letters) >NCBI__GCF_000757425.2:WP_038021191.1 Length = 484 Score = 628 bits (1619), Expect = 0.0 Identities = 312/477 (65%), Positives = 372/477 (77%) Query: 3 LNDPSLLRQQCYINGQWCDANSKETVAITNPATGAVIACVPVMGQAETQAAIAAAEAALP 62 L+DPSLLR+ C + G+W A T+A+ NPAT +IA VP + QAE + A+ +A+ A Sbjct: 4 LDDPSLLRETCLLAGEWRSAADGATLAVNNPATLDIIAHVPRLAQAEVEQAVVSAQQAFE 63 Query: 63 AWRALTAKERGAKLRRWFELLNENSDDLALLMTSEQGKPLTEAKGEVTYAASFIEWFAEE 122 WR TA +R A LRRWFEL+ ENS+DLA +MT+EQGKPL E++GEV+YAASFIEWFAEE Sbjct: 64 QWRQQTAGQRCALLRRWFELITENSEDLAAIMTAEQGKPLAESRGEVSYAASFIEWFAEE 123 Query: 123 AKRIYGDTIPGHQGDKRIMVIKQPVGVTAAITPWNFPAAMITRKAAPALAAGCTMVVKPA 182 KR YGD IP Q DKR++VIKQPVGV AAITPWNFPAAMITRKA PALAAGC M+VKPA Sbjct: 124 GKRTYGDVIPPTQADKRLLVIKQPVGVCAAITPWNFPAAMITRKAGPALAAGCVMIVKPA 183 Query: 183 PQTPFTALALAVLAERAGIPAGVFSVITGDAIAIGNEMCTNPIVRKLSFTGSTNVGIKLM 242 QTP TALAL LA RAGIPAGV VITGD+ IG + + +VRKLSFTGST +G LM Sbjct: 184 KQTPLTALALGELAMRAGIPAGVLQVITGDSKVIGGVLTRSDVVRKLSFTGSTAIGRSLM 243 Query: 243 AQCAPTLKKLSLELGGNAPFIVFDDANIDAAVEGAMIAKYRNAGQTCVCANRIYVQAGVY 302 A CAPTLK+LSLELGGNAPFIVFDDAN++ AVEGA+ +KYRNAGQTCVC NR VQ+G+Y Sbjct: 244 ADCAPTLKRLSLELGGNAPFIVFDDANLEEAVEGALQSKYRNAGQTCVCTNRFLVQSGIY 303 Query: 303 DEFAEKLSMAVAKLKVGEGIIAGVTTGPLINAAAVEKVQSHLEDAIKKGATVLAGGKVHE 362 D FA++L+ VA+LK+G+G GV GPLI+ AV KVQ HL+DA +KG V GG+ Sbjct: 304 DRFAQRLAERVAELKIGDGTDEGVQIGPLIDENAVVKVQQHLKDAQQKGGQVTTGGERLT 363 Query: 363 LGGNFFEPTVLTNADKSMRVAREETFGPLAPLFKFNDVDDVIKQANDTEFGLAAYFYGRD 422 G F P V+ NAD+ M VAREETFGP+APLF+F+ I+ ANDTEFGLAAYFY + Sbjct: 364 PEGLFITPAVIVNADREMLVAREETFGPVAPLFRFDTEQQAIEMANDTEFGLAAYFYTEN 423 Query: 423 ISLVWKVAESLEYGMVGVNTGLISTEVAPFGGMKSSGLGREGSKYGIEEYLEIKYIC 479 +W+V+E+LEYGMVG NTGLIS EVAPFGG+K SG+GREGSKYGI+EYLEIKY+C Sbjct: 424 SRRMWRVSEALEYGMVGHNTGLISNEVAPFGGIKQSGIGREGSKYGIDEYLEIKYLC 480 Lambda K H 0.318 0.133 0.390 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: 698 Number of extensions: 15 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: 482 Length of database: 484 Length adjustment: 34 Effective length of query: 448 Effective length of database: 450 Effective search space: 201600 Effective search space used: 201600 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