GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Thiomicrospira cyclica ALM1

Align succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_013835847.1 THICY_RS06630 aspartate aminotransferase family protein

Query= BRENDA::O30508
         (406 letters)



>NCBI__GCF_000214825.1:WP_013835847.1
          Length = 390

 Score =  272 bits (695), Expect = 1e-77
 Identities = 156/378 (41%), Positives = 226/378 (59%), Gaps = 18/378 (4%)

Query: 31  GEGSRVWDQSGRELIDFAGGIAVTSLGHAHPALVKALTEQAQRIWHVSNVFTNEPALRLA 90
           GEG+ ++D+     +D   GIAV SLGHAHPA+ +AL EQ++ + H SN++      +L 
Sbjct: 18  GEGALLYDEQDNAYLDAVSGIAVCSLGHAHPAIAQALCEQSKTLIHTSNLYHVAKQQQLG 77

Query: 91  RKLVDATFAERVFLANSGAEANEAAFKLARRYANDVYGPQKYEIIAASNSFHGRTLFTVN 150
            KLV  +  ++VF  NSGAEANEAA K+AR+Y +   G    +II   NSFHGRTL T++
Sbjct: 78  DKLVAISGMDKVFFGNSGAEANEAAIKMARKYGHSK-GISHAQIIVMENSFHGRTLATLS 136

Query: 151 VGGQPKYSDGFGPKFEGITHVPYNDLEALKAAISDK--TCAVVLEPIQGEGGVLPAQQAY 208
             G  K  DGF P  EG   VP++++EA+  AI++     A+++EP+QGEGGV   +  Y
Sbjct: 137 ATGSAKVHDGFYPLVEGFVRVPFDNVEAVANAIANNPNVVAILVEPVQGEGGVHVPKPGY 196

Query: 209 LEGARKLCDEHNALLVFDEVQSGMGRVGELFAYMHYGVVPDILSSAKSLGGGFPIGAMLT 268
           L+  R LCDEH+ LL+ DE+Q+G+GR G+ FA+ H G++PD+LS AK+LG G PIGA L 
Sbjct: 197 LKALRALCDEHDLLLMIDEIQAGIGRTGKWFAFQHEGILPDVLSLAKALGNGVPIGASLA 256

Query: 269 TGEIAKHLSVGTHGTTYGGNPLASAVAEAALDVINTPEVLDGVKAKHER----FKSRLQK 324
            G+ A+  + G HGTT+GGNPLA A   A ++ +     +D V  +       FK+ L  
Sbjct: 257 RGKAAELFAPGNHGTTFGGNPLACAAGLAVIETLEYHNYIDLVAKQGAELLAAFKTALAN 316

Query: 325 IGQEYGIFDEIRGMGLLIGAALTDEWKGKARDVLNAAEKEAVMVLQASPDVVRFAPSLVI 384
           I    G+ D IRG G +IG  L         D++  A  + +++     D VR  P+ V+
Sbjct: 317 IP---GVVD-IRGKGYMIGIQL----DRPCGDLVKMALADKLLINVTRGDTVRLLPTFVM 368

Query: 385 DDAEIDE---GLERFERA 399
             A+ ++   GL R  +A
Sbjct: 369 THAQSEQLVNGLTRLIKA 386


Lambda     K      H
   0.318    0.135    0.394 

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: 413
Number of extensions: 25
Number of successful extensions: 3
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: 406
Length of database: 390
Length adjustment: 31
Effective length of query: 375
Effective length of database: 359
Effective search space:   134625
Effective search space used:   134625
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: 50 (23.9 bits)

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

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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