Align succinate-semialdehyde dehydrogenase (NAD+) (EC 1.2.1.24); glyceraldehyde-3-phosphate dehydrogenase (NADP+) (EC 1.2.1.9) (characterized)
to candidate WP_038806127.1 HK29_RS05075 NADP-dependent glyceraldehyde-3-phosphate dehydrogenase
Query= BRENDA::Q97XS9 (470 letters) >NCBI__GCF_000382825.1:WP_038806127.1 Length = 474 Score = 287 bits (734), Expect = 6e-82 Identities = 172/464 (37%), Positives = 261/464 (56%), Gaps = 10/464 (2%) Query: 3 SQEVIEVRSPSNLNVIGTVKRMHKDEVRGEIEEAYKGFEIISKMPLYKRTAILRKVSEIL 62 S++ I + SP N +GTV M + EV ++ A + +R A L K ++IL Sbjct: 15 SEKEITIYSPINQEKLGTVPAMSQAEVDEAMKAARAALPAWRDLAPVERAAYLHKTADIL 74 Query: 63 EREQERLAKLLAMEAGKPIRDSRVEVLRASRLFRHAAEEVGMVLEGKNYRVDAYEYPPGN 122 ER++E++ +LA E K I+ + EV+R + L R AAEE G+ + G+ +E + Sbjct: 75 ERDKEKIGTILAKEVAKGIKAAIGEVVRTADLIRFAAEE-GLRITGQAMEGGGFE--AAS 131 Query: 123 ENRIVVSTREPIGVVTAILPFNFPINSFAHKVAPALAVGNSVVVKPSINTPLAAIEMKKI 182 +N++ V REP+GVV AI PFN+P+N K+APAL GN V+ KP ++ + + K Sbjct: 132 KNKLAVVRREPVGVVLAIAPFNYPVNLSGSKIAPALIAGNVVMFKPPTQGSISGLLLAKA 191 Query: 183 LVEAGLPDSAVRVVTGYSSEIGDEIITHPLVGLITLTGSTQTGLKIASKAVSLGKR-IIM 241 EAG+P +TG SEIGD II H V I TGST G +I A G R I++ Sbjct: 192 FDEAGIPAGVFNTITGRGSEIGDYIIEHKEVNFINFTGSTPIGERIGRLA---GMRPIML 248 Query: 242 ELGGSDPIIILEDANIERASSIAVRARFEYAGQNCNAGKRIIVREEIYDKFVKAFNDKAR 301 ELGG D I+LEDA++E A+ V F Y+GQ C A KR++V E + D+ + + Sbjct: 249 ELGGKDAAIVLEDADLEHAAKQIVGGAFSYSGQRCTAIKRVLVVESVADRLAELLQAEVA 308 Query: 302 ALKVGDPLDETTDVGPVINKESVENLNSVLADAKAKGGKVEILNKGPESGSFFPLTMVTN 361 L VGDP D D+ PV++ S + + ++ DA+ KG K L+ G+ + Sbjct: 309 KLTVGDPFD-NADITPVVDNASADFIWGLIQDAQEKGAKA--LSPIKREGNLIWPGLFDY 365 Query: 362 PSLDMLVLKSEVFGPIVPIVSVKSDEEAIRIANSTEYGLQSAIFTNDVNRALKLSRELKF 421 + DM + E+FGP++PI+ V EA+ IAN +E+GLQS++FTND +A +++ +L+ Sbjct: 366 VTRDMKLAWEELFGPVLPIIRVADANEAVAIANESEFGLQSSVFTNDFKKAFEIAEKLEV 425 Query: 422 GAVIINDSTRLRWDSLAFGGFKKSSIGREGVRETMLEMTENKLI 465 G V IN+ T+ D+ F G K S G +G++ ++ MT K I Sbjct: 426 GTVHINNKTQRGPDNFPFLGVKGSGAGVQGIKYSIEAMTNVKSI 469 Lambda K H 0.316 0.134 0.365 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: 534 Number of extensions: 28 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: 470 Length of database: 474 Length adjustment: 33 Effective length of query: 437 Effective length of database: 441 Effective search space: 192717 Effective search space used: 192717 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: 51 (24.3 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