Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_004511896.1 GMET_RS09835 phosphoglycerate kinase
Query= BRENDA::P36204 (654 letters) >NCBI__GCF_000012925.1:WP_004511896.1 Length = 398 Score = 415 bits (1067), Expect = e-120 Identities = 218/402 (54%), Positives = 281/402 (69%), Gaps = 10/402 (2%) Query: 4 MTIRDVD----LKGKRVIMRVDFNVPVKDGV-VQDDTRIRAALPTIKYALEQGAKVILLS 58 M IR +D LKGK+V +RVDFNVP+ + + +DTRIRA LPTI +AL+ GAKVIL S Sbjct: 1 MAIRYIDEIESLKGKKVFIRVDFNVPLDEHQNITEDTRIRAVLPTINFALDAGAKVILAS 60 Query: 59 HLGRPKGEPSPEFSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTR 118 HLGRPKGE P++S+AP AKRLS LL KEV+ P +GDEVKK ++ +K GEVLLLEN R Sbjct: 61 HLGRPKGERKPKYSMAPAAKRLSRLLNKEVQLAPDCIGDEVKKMIDAMKPGEVLLLENVR 120 Query: 119 FHPGETKNDPELAKFWASLADIHVNDAFGTAHRAHASNVGIAQFIPSV-AGFLMEKEIKF 177 F+ GE KND + AK A+ +I++NDAF +HRAHAS I +F P V AGFLM EI + Sbjct: 121 FYEGEEKNDADFAKALANDCEIYINDAFAVSHRAHASVEAITKFFPVVAAGFLMNNEINY 180 Query: 178 LSKVTYNPEKPYVVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSR 237 K P +P V +LGGAKVS K+ V+ +L+ K D+I+IGG M FTFLKALG VG S Sbjct: 181 FEKAMQKPIRPLVAILGGAKVSGKLEVLESLVNKVDKIIIGGGMAFTFLKALGYNVGKSL 240 Query: 238 VEEDKIDLAKELLEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIG 297 VEE+ +++A KA+EKGV+ LPVD V A + P E KV I + IPE WM LDIG Sbjct: 241 VEEELLEIALTTYTKAREKGVKFYLPVDCVAADRFNPEAETKVTTIQE-IPEEWMALDIG 299 Query: 298 PETIELFKQKLSDAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDSA 357 P T+ LF + L +AKT++WNGPMGVFE+D F+ GT + ++A+ A+T+VGGGD+ Sbjct: 300 PATVTLFTEALQNAKTIIWNGPMGVFEMDAFSRGTFAM---VSAVANSYALTIVGGGDTD 356 Query: 358 AAVNKFGLEDKFSHVSTGGGASLEFLEGKELPGIASIADKKK 399 +AV++ G K S++STGGGA LE LEGK LPGI + + K Sbjct: 357 SAVHRAGEYAKISYISTGGGAFLELLEGKHLPGIKVLEENGK 398 Lambda K H 0.317 0.137 0.386 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: 622 Number of extensions: 33 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: 654 Length of database: 398 Length adjustment: 34 Effective length of query: 620 Effective length of database: 364 Effective search space: 225680 Effective search space used: 225680 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: 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