GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Haloechinothrix alba DSM 45207

Align L-threonine aldolase (EC 4.1.2.5) (characterized)
to candidate WP_089302170.1 CHB84_RS14645 low specificity L-threonine aldolase

Query= BRENDA::Q9X266
         (343 letters)



>NCBI__GCF_900188115.1:WP_089302170.1
          Length = 360

 Score =  251 bits (641), Expect = 2e-71
 Identities = 145/337 (43%), Positives = 207/337 (61%), Gaps = 13/337 (3%)

Query: 1   MIDLRSDTVTKPTEEMRKAMAQAEVGDDVYGEDPTINELERLAAETFGKEAALFVPSGTM 60
           +IDLRSDT+T P E MR AMA AEVGD+V   DPT+  LE+  A+  GK AAL+ PSGTM
Sbjct: 8   LIDLRSDTLTVPDEPMRAAMAGAEVGDNVLDGDPTVRALEQRTAQLLGKPAALWTPSGTM 67

Query: 61  GNQVSIMAHTQRGDEVILEADSHIFWYEVGAMAVLSGVMPHPV-----PGKNGAMDPDDV 115
            N +++  H QRGD  +   D+H+   E+G+ A L+G MP  +     PG+      + +
Sbjct: 68  ANVIALCLHLQRGDRFLAPRDAHVLLNELGSAAWLAGGMPEAIGTDLGPGRPSPHTLERI 127

Query: 116 RKAIRPRNIHFPRTSLIAIENTHNRSGGRVVPLENIKEICTIAKEHGINVHIDGARIFNA 175
             A R    +  RTSL+ +ENTHN +GG V+P +   ++   A++ G++VH+DGAR++NA
Sbjct: 128 ISAGRNAPYYALRTSLLCLENTHNAAGGAVIPADEHAQLVATARDGGLSVHLDGARLWNA 187

Query: 176 SIASGVPVKEYAGYADSVMFCLSKGLCAPVGSVVVGDRDFIERARKARKMLGGGMRQAGV 235
           ++A  VP       ADSV  C SKGL APVGS + G  +FIE AR+ R+MLGGG+RQ GV
Sbjct: 188 AVALNVPPAALTVGADSVSVCFSKGLGAPVGSALAGSAEFIEHARRTRQMLGGGVRQGGV 247

Query: 236 LAAAGIIALTKMVDRLKEDHENARFLALKLKEIGYSVNPEDVKTNMVILRTDNLKVNAHG 295
           LAA+ + AL +M D L  DH NA  LA  L ++G+ V     +TN+V+    +++   H 
Sbjct: 248 LAASCLKALDRM-DELATDHANAARLASGLSDLGWDV--PTPQTNIVLGAVADVERTLH- 303

Query: 296 FIEALRNSGVLANAVSDTEIRLVTHKDVSRNDIEEAL 332
              +LR   +LA  ++   +R V H+ ++   IEEAL
Sbjct: 304 ---SLRELDILAMPMAG-RVRFVVHRAITSAVIEEAL 336


Lambda     K      H
   0.319    0.135    0.384 

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: 314
Number of extensions: 14
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: 343
Length of database: 360
Length adjustment: 29
Effective length of query: 314
Effective length of database: 331
Effective search space:   103934
Effective search space used:   103934
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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