Align glutamate dehydrogenase (EC 1.4.1.2) (characterized)
to candidate WP_084932454.1 HA51_RS04670 Glu/Leu/Phe/Val dehydrogenase
Query= BRENDA::P27346 (421 letters) >NCBI__GCF_002095475.1:WP_084932454.1 Length = 424 Score = 397 bits (1020), Expect = e-115 Identities = 196/408 (48%), Positives = 271/408 (66%), Gaps = 5/408 (1%) Query: 14 SQVKNACDKLGMEPAVYELLKEPMRVIEVSIPVKMDDGSIKTFKGFRSQHNDAVGPTKGG 73 +QV LG + L+ P R V IP++MDDG+++ F+GFR QHN + GP KGG Sbjct: 21 AQVDRVMPYLGDLSRWADTLRHPKRAFIVDIPLEMDDGTVRHFEGFRVQHNLSRGPGKGG 80 Query: 74 IRFHQNVSRDEVKALSIWMTFKCSVTGIPYGGGKGGIIVDPSTLSQGELERLSRGYIDGI 133 IR+H +V+ +EV ALS WMT KC+V +P+GG KGGI VDP LS ELERL+R Y I Sbjct: 81 IRYHPDVNLEEVMALSAWMTVKCAVINLPFGGAKGGIRVDPRELSIKELERLTRRYTSEI 140 Query: 134 YKLIGEKVDVPAPDVNTNGQIMSWMVDEYNKLTGQSSIGVITGKPVEFGGSLGRTAATGF 193 +IG + D+PAPDV TN Q+M+W++D ++ G +S GV+TGKPV GGSLGR ATG Sbjct: 141 GNIIGPQRDIPAPDVGTNAQVMAWIMDTWSMNAGATSTGVVTGKPVHLGGSLGRVTATGR 200 Query: 194 GVAVTAREAAAKLGIDMKKAKIAVQGIGNVGSYTVLNCEKLGGTVVAMAEWCKSEGSYAI 253 GV VT R AA +G+ ++++++AVQG GNVGS V ++ G +VA+ + S + Sbjct: 201 GVFVTGRAAAKNIGLTVERSRVAVQGFGNVGSVAVGLFQEAGAHIVAV-----QDHSTTL 255 Query: 254 YNENGLDGQAMLDYMKEHGNLLNFPGAKRISLEEFWASDVDIVIPAALENSITKEVAESI 313 +N G+D A+ + ++HG + FPGA+ IS E+FW D DI+IPAALE IT E A + Sbjct: 256 WNNEGIDIPALQSWQQKHGAIAGFPGARVISSEDFWLKDFDILIPAALEGQITAERAHKL 315 Query: 314 KAKLVCEAANGPTTPEADEVFAERGIVLTPDILTNAGGVTVSYFEWVQNLYGYYWSEEEV 373 KLV E ANGPT PEAD++ +RG+ + PD+L NAGGVTVSYFEWVQ+ Y+W E+E+ Sbjct: 316 TCKLVLEGANGPTLPEADDILRQRGVTIVPDVLCNAGGVTVSYFEWVQDFSSYFWGEDEI 375 Query: 374 EQKEEIAMVKAFESIWKIKEEYNVTMREAAYMHSIKKVAEAMKLRGWY 421 + ++ M +AFE++W+ E VT+R AAY +++ A K RG Y Sbjct: 376 NSRLDMIMSQAFEAVWQKAESLGVTLRTAAYAVGCERILIARKERGIY 423 Lambda K H 0.315 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: 470 Number of extensions: 15 Number of successful extensions: 2 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: 421 Length of database: 424 Length adjustment: 32 Effective length of query: 389 Effective length of database: 392 Effective search space: 152488 Effective search space used: 152488 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: 42 (22.0 bits) S2: 50 (23.9 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