Align 2-hydroxymuconate-6-semialdehyde dehydrogenase (EC 1.2.1.85) (characterized)
to candidate GFF1133 HP15_1111 betaine aldehyde dehydrogenase
Query= BRENDA::Q1XGK8 (486 letters) >FitnessBrowser__Marino:GFF1133 Length = 493 Score = 850 bits (2195), Expect = 0.0 Identities = 405/486 (83%), Positives = 444/486 (91%) Query: 1 MKEIKHFINGAFVGSASGRTFEDINPSNGQVIGHVHEAGRAEVDAAVKAARAALKGPWGK 60 MKEIKH ING +V S S R F+++NP+NG++I VHEAGR EVDAAVKAARAAL+GPWGK Sbjct: 8 MKEIKHHINGQYVSSCSSRLFDNVNPANGKIISKVHEAGREEVDAAVKAARAALRGPWGK 67 Query: 61 LSVAERAEILHRVADGITARFDEFLEAECLDTGKPKSLASHIDIPRGAANFKVFADLLKN 120 +++ ER ILH+VADGI ARFDEFLE ECLDTGKPKS+ASHIDIPRGAANFKVFAD++KN Sbjct: 68 MTLDERTSILHKVADGINARFDEFLEGECLDTGKPKSMASHIDIPRGAANFKVFADMIKN 127 Query: 121 VANEAFEMATPDGAGAINYAVRRPKGVIGVISPWNLPLLLMTWKVGPALACGNTVVVKPS 180 V E+FEM TPDG GA+NYAVRRPKGVIGVISPWNLPLLLMTWKVGPALACGNTVVVKPS Sbjct: 128 VPTESFEMPTPDGTGALNYAVRRPKGVIGVISPWNLPLLLMTWKVGPALACGNTVVVKPS 187 Query: 181 EETPLTATLLGEVMQAAGVPAGVYNVVHGFGGDSAGAFLTEHPDVDAYTFTGETGTGEVI 240 EETP T TLLGEVM+ AGVP GV+NVVHGFGGDSAGAFLTEHP VD TFTGE GTGEVI Sbjct: 188 EETPTTTTLLGEVMKEAGVPDGVFNVVHGFGGDSAGAFLTEHPQVDGITFTGEIGTGEVI 247 Query: 241 MRAAAKGVRQVSLELGGKNAGIVFADCDMDKAIEGTLRSAFANCGQVCLGTERVYVERPI 300 M+AAAKG+R +SLELGGKNAG+VFADCD+DKAIEGT+RSAFANCGQVCLGTERVYVER I Sbjct: 248 MKAAAKGIRDISLELGGKNAGVVFADCDIDKAIEGTMRSAFANCGQVCLGTERVYVERSI 307 Query: 301 FDEFVARLKAGAESLMIGPPDDASSNFGPLVSLKHREKVLSYYQQAVDDGGSVITGGGVP 360 FDEFV RLK AE + IGPPDDA ++ GPLVSL HREKVLSYYQ+AVDDG +V+TGGGVP Sbjct: 308 FDEFVGRLKEAAEGMKIGPPDDAEADMGPLVSLNHREKVLSYYQKAVDDGATVVTGGGVP 367 Query: 361 DMPAHLAGGAWVQPTIWTGLSDDSAVVTEEIFGPCCHIRPFDTEEEAIELANSLPYGLAS 420 +MP LAGGAWVQPTIWTGL +DSAV+T+EIFGPCCHIRPFDTEEEAIELANSLPYGLAS Sbjct: 368 EMPEALAGGAWVQPTIWTGLPEDSAVITDEIFGPCCHIRPFDTEEEAIELANSLPYGLAS 427 Query: 421 AIWTENGSRAHRVAGQIEAGIVWVNSWFLRDLRTAFGGSKQSGIGREGGVHSLEFYTELK 480 AIW+EN +RAHRVAGQIEAGI+WVNSWFLRDLRT FGGSKQSGIGREGGVHSLEFYTE+K Sbjct: 428 AIWSENITRAHRVAGQIEAGIIWVNSWFLRDLRTPFGGSKQSGIGREGGVHSLEFYTEMK 487 Query: 481 NICVKL 486 NICVKL Sbjct: 488 NICVKL 493 Lambda K H 0.318 0.136 0.411 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: 913 Number of extensions: 21 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: 486 Length of database: 493 Length adjustment: 34 Effective length of query: 452 Effective length of database: 459 Effective search space: 207468 Effective search space used: 207468 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