Align putative hydrolase, required for lysine catabolism (characterized)
to candidate GFF3040 PS417_15555 hypothetical protein
Query= reanno::pseudo5_N2C3_1:AO356_01105 (458 letters) >FitnessBrowser__WCS417:GFF3040 Length = 458 Score = 698 bits (1801), Expect = 0.0 Identities = 355/453 (78%), Positives = 385/453 (84%), Gaps = 3/453 (0%) Query: 4 VSPDLIRQRFSRAMSDMYRDEVPLYGALMKLVEHTNAQVLSEQPQLAEHLRSTGELERLD 63 VSPD IR+ FS+AMSDMYRDEVPLYGALM+LV TNA VL QPQLA+ L+ TGE++RLD Sbjct: 7 VSPDQIRRGFSKAMSDMYRDEVPLYGALMELVAETNAHVLDTQPQLAQQLQRTGEIQRLD 66 Query: 64 LERHGAIRVGTAAELATLGRLFAVMGMQPVGYYDLTPAGVPVHSTAFRAVHESALQVSPF 123 +ERHGAIR+GTAAELAT+ RLFAVMGMQPVGYYDLTPAGVPVHSTAFRAVHE ALQ SPF Sbjct: 67 MERHGAIRLGTAAELATISRLFAVMGMQPVGYYDLTPAGVPVHSTAFRAVHEQALQTSPF 126 Query: 124 RVFTSLLRLELIENSELRAFAESVLAKRQIFTPGALALIDLAERQGGLTQAQAEDFVLQA 183 RVFTSLLRLELIEN +LRAFAE+ LAKR IFT GAL LI+ AE+ GGL A++F+ QA Sbjct: 127 RVFTSLLRLELIENPDLRAFAETALAKRSIFTRGALTLIEQAEKDGGLNAEDADEFIRQA 186 Query: 184 LETFRWHHSATVTAEQYRQLSAQHRLIADVVAFKGPHINHLTPRTLDIDIVQARMPVHGI 243 LETFRWHH+ATVT QY+QLS QHRLIADVVAFKGPHINHLTPRTLDID VQA MP GI Sbjct: 187 LETFRWHHTATVTGAQYQQLSDQHRLIADVVAFKGPHINHLTPRTLDIDQVQAAMPGKGI 246 Query: 244 TPKAVIEGPPRRQCPILLRQTSFKALDEPVAFTDQPQAQGSHSARFGEIEQRGAALTPKG 303 TPKAVIEGPPRR CPILLRQTSFKALDEP+AFTD AQGSHSARFGEIEQRG ALTPKG Sbjct: 247 TPKAVIEGPPRRHCPILLRQTSFKALDEPIAFTD---AQGSHSARFGEIEQRGVALTPKG 303 Query: 304 RALYDQLLNAARDALGAFPNEANAERYNALMTEHFVAFPDNHDELRQQALAYFRYFPTPK 363 RALYDQLLNAARD LGAFPNE NA RY LM HF AFPDNH ++R+Q LAYFRYF T + Sbjct: 304 RALYDQLLNAARDELGAFPNEGNAARYVELMERHFQAFPDNHAQMREQGLAYFRYFATEQ 363 Query: 364 GLAAKGTLEPAASLEHLLEQQYLRAEPLVYEDFLPVSAAGIFQSNLGDAAQSHYAGQSNR 423 GLAA+GT +LE L+E ++ EPLVYEDFLPVSAAGIFQSNLGDAAQSHYA SNR Sbjct: 364 GLAARGTAAQPRTLEALVEASHIDVEPLVYEDFLPVSAAGIFQSNLGDAAQSHYAANSNR 423 Query: 424 QAFEAALGRATIDELGLYAQTQQRSIDECRAAL 456 FE ALGR TIDEL LY +TQQRSIDEC AL Sbjct: 424 AEFEKALGRRTIDELKLYGETQQRSIDECTKAL 456 Lambda K H 0.320 0.134 0.383 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: 739 Number of extensions: 20 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: 458 Length of database: 458 Length adjustment: 33 Effective length of query: 425 Effective length of database: 425 Effective search space: 180625 Effective search space used: 180625 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: 51 (24.3 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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