Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_041376699.1 PNAP_RS13165 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000015505.1:WP_041376699.1 Length = 490 Score = 295 bits (756), Expect = 2e-84 Identities = 166/468 (35%), Positives = 264/468 (56%), Gaps = 6/468 (1%) Query: 11 IDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERAS 70 I+GQ++ G + DV +P+ ++ + + DA AI AA A P W ER+ Sbjct: 23 INGQWLA--GASRFDVSDPSNGNKLADVANLGPADAEAAIAAANAAWPAWRGKTGKERSI 80 Query: 71 WLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQSD 130 LRK + +++ ++ E GK A+ EVA+ A ++++ AE A+R GE + Sbjct: 81 ILRKWFDLLMANQEDLARIMTAEQGKPFAEAKGEVAYGASFVEWFAEEAKRVNGETLPQF 140 Query: 131 RPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFAK 190 +++ K+ +GV I PWNFP +I RK+APAL G T+VIKP+E TP A+A + Sbjct: 141 DNNRRLMVLKQPIGVCVAITPWNFPLAMITRKVAPALAAGCTVVIKPAELTPLTALAAVE 200 Query: 191 IVDEIGLPRGVFN-LVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKVC 249 + G+P GV N L VG+ + V +S TGS G +MA +A +I K+ Sbjct: 201 LAVRAGVPSGVLNILTTDESAAVGKVFCASDVVRHISFTGSTEVGRILMAQSAPSIKKLS 260 Query: 250 LELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEAM 309 LELGG AP IV DDAD++ AV+ + S+ N+GQ C CA R+YVQ+G+YDQFV++ E + Sbjct: 261 LELGGNAPFIVFDDADIDSAVEGAMASKYRNAGQTCVCANRIYVQEGVYDQFVHKFAEKV 320 Query: 310 QAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPPTL 369 + ++ GN E + + GPLI AA+ +VE+ V A+ +G ++ GG +EG+ ++ PT+ Sbjct: 321 RLLKVGNGFE-DGVGQGPLIEDAAVHKVERHVQDALAKGGKLLAGGHKLEGQ--FFEPTV 377 Query: 370 LLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIKG 429 + + +M EETFGP PV F ++AI AN++++GL S Y++++ + + Sbjct: 378 ISEAHADMLCAREETFGPFAPVFRFTHEQEAIDAANNTEFGLASYFYSRDIGRIYRVAEA 437 Query: 430 LKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYL 477 L++G IN G ++SG+G HG+ EYL+ + + L Sbjct: 438 LEYGMVGINAGVIATEHVPFGGVKQSGLGREGSSHGMEEYLEIKYLCL 485 Lambda K H 0.318 0.135 0.392 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: 546 Number of extensions: 25 Number of successful extensions: 5 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: 479 Length of database: 490 Length adjustment: 34 Effective length of query: 445 Effective length of database: 456 Effective search space: 202920 Effective search space used: 202920 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 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