GapMind for catabolism of small carbon sources

 

Aligments for a candidate for HSERO_RS00870 in Herbaspirillum seropedicae SmR1

Align Branched chain amino acid ABC transporter substrate-binding protein (characterized, see rationale)
to candidate HSERO_RS08270 HSERO_RS08270 amino acid ABC transporter substrate-binding protein

Query= uniprot:A0A165KTD4
         (375 letters)



>lcl|FitnessBrowser__HerbieS:HSERO_RS08270 HSERO_RS08270 amino acid
           ABC transporter substrate-binding protein
          Length = 373

 Score =  185 bits (469), Expect = 2e-51
 Identities = 129/371 (34%), Positives = 193/371 (52%), Gaps = 23/371 (6%)

Query: 11  AAIAAAAGVASAQEQVVKIGHVAPVSGAQAHYGKDNENGARMAIEELNAQGVTIGGKKIK 70
           A  AA AGVA A+   VKI    P++GA A YG   + GA  AIE++NA G   G    K
Sbjct: 15  ATFAAFAGVAHAE--TVKIAIAGPMTGAVAQYGDMVKAGALTAIEQINAAG---GANGNK 69

Query: 71  FELVAEDDAADPKQGTAAAQKLCDAKVAGVVGHLNSGTTIPASKVYNDCGIPHVTGAATN 130
           FE V  DDA +PKQ  A A K+    +  V+GH+ SG+TIPAS +Y + G+  +T +AT 
Sbjct: 70  FEAVMMDDACEPKQAVAVANKIVSQGIKYVIGHVCSGSTIPASDIYENEGVVMITPSATA 129

Query: 131 PNLT--KPGYKTTFRIIANDNALGAGLAFYAVDTLKLKTVAIIDDRTAYGQGVADVFKKT 188
           P LT  KP +K  FR I  D+  G   A Y ++ LK K VA++ D+ +YGQGVA   K  
Sbjct: 130 PQLTEAKP-HKFIFRTIGRDDQQGPAAARYVIEKLKPKKVAVLHDKQSYGQGVASSVKAA 188

Query: 189 ATAKGMKVVDEQFTTDKATDFMAILTAIKAKNPDAIFYGGMDPQGGPMLRQMEQLGMGNV 248
             A  + VV  +      +D+ AI+T +K++  D +++GG  P+ G ++RQ  + G+  V
Sbjct: 189 LDAAKVPVVVFEGINAGDSDYSAIVTKLKSQGVDFVYFGGYHPEMGLIMRQAREQGIKAV 248

Query: 249 KYFGGDGICTSEIAKLAAGAKTLGNVICAEGGSSLAKMPGGTAW-----KAKYDAKYPNQ 303
            + G +G+   +I  + AG  + G ++     +  A  P   A       AK D   P Q
Sbjct: 249 -FMGPEGVGNKDITAI-AGPASEGMLVTLP--ADFAADPANAALVKAFAAAKRDPNGPFQ 304

Query: 304 FQVYSPYTYDATFLIVDAMKRANSVDPKVYTPELAKSSFKGVTSTIAFEPNGEMKNPAIT 363
              YS        +I DA+  A S DP+     +  +SFK     + ++  G++K+    
Sbjct: 305 MPAYS-----GVKIIADAIAGAKSTDPEKVAAYIHANSFKTPIGNVEYDKKGDLKSFKFV 359

Query: 364 LYV-YKDGKKT 373
           ++  +KD  KT
Sbjct: 360 VFTWHKDASKT 370


Lambda     K      H
   0.315    0.131    0.375 

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: 395
Number of extensions: 23
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 375
Length of database: 373
Length adjustment: 30
Effective length of query: 345
Effective length of database: 343
Effective search space:   118335
Effective search space used:   118335
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: 42 (22.0 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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 the paper from 2019 on GapMind for amino acid biosynthesis, or view the source code.

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