Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_012852549.1 TCUR_RS10895 phosphoglycerate kinase
Query= BRENDA::P36204 (654 letters) >NCBI__GCF_000024385.1:WP_012852549.1 Length = 395 Score = 407 bits (1047), Expect = e-118 Identities = 219/397 (55%), Positives = 278/397 (70%), Gaps = 9/397 (2%) Query: 5 TIRDVDLKGKRVIMRVDFNVPVKDGVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRPK 64 TI D+D++GKRV++R D NVP+ + DD RIRA+LPTI E+GAKVI+ +HLGRPK Sbjct: 3 TIDDLDVRGKRVLVRSDLNVPLDGDRITDDGRIRASLPTINTLRERGAKVIVCAHLGRPK 62 Query: 65 GEPSPEFSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGET 124 G+ PEFSLAPVA+RL ELLG EV F VVG+ + V L +G+V LLEN RF PGET Sbjct: 63 GQVKPEFSLAPVARRLGELLGTEVAFASDVVGESAARTVAGLADGQVALLENLRFEPGET 122 Query: 125 -KNDPELAKF---WASLADIHVNDAFGTAHRAHASNVGIAQFIPSVAGFLMEKEIKFLSK 180 K+D E F A+LAD++V D FG HR HAS + + +P AG L+ E+ L K Sbjct: 123 SKDDAERGAFADKLAALADLYVGDGFGAVHRKHASVYDVPRRLPHAAGGLIVAEVDVLRK 182 Query: 181 VTYNPEKPYVVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEE 240 +T E+PY VVLGG+KVSDK+GVI NL+ KADRILIGG M+FTFL A G +VG S +E+ Sbjct: 183 LTEEVERPYAVVLGGSKVSDKLGVIDNLLNKADRILIGGGMVFTFLAAQGHQVGKSLLEQ 242 Query: 241 DKIDLAKELLEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPET 300 D++D +E L +A++ GVE+VLPVD V A + +VV D IP MGLDIGP + Sbjct: 243 DQLDTVREYLARAEKNGVELVLPVDIVAATAFAADADHQVVPA-DAIPADRMGLDIGPAS 301 Query: 301 IELFKQKLSDAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDSAAAV 360 LF ++L+ AKTV WNGPMGVFE++ ++ GT+ VA L + GA TVVGGGDSAAAV Sbjct: 302 GRLFAERLAGAKTVFWNGPMGVFEMEPYSHGTRAVA---QGLIDSGAFTVVGGGDSAAAV 358 Query: 361 NKFGL-EDKFSHVSTGGGASLEFLEGKELPGIASIAD 396 G E FSH+STGGGASLE+LEGK LPG+A++ D Sbjct: 359 RSLGFDESAFSHISTGGGASLEYLEGKTLPGLAALED 395 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: 671 Number of extensions: 37 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: 395 Length adjustment: 34 Effective length of query: 620 Effective length of database: 361 Effective search space: 223820 Effective search space used: 223820 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 Jul 25 2024. The underlying query database was built on Jul 25 2024.
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