Alignments for a candidate for PS417_11890 in Herbaspirillum seropedicae SmR1

GapMind for catabolism of small carbon sources

Alignments for a candidate for PS417_11890 in Herbaspirillum seropedicae SmR1

Align Inositol transport system ATP-binding protein (characterized)
to candidate HSERO_RS22465 HSERO_RS22465 sugar ABC transporter

Query= reanno::WCS417:GFF2332
         (517 letters)



>FitnessBrowser__HerbieS:HSERO_RS22465
          Length = 518

 Score =  390 bits (1002), Expect = e-113
 Identities = 220/500 (44%), Positives = 315/500 (63%), Gaps = 11/500 (2%)

Query: 22  YLLEIVNISKGFPGVVALADVQLRVRPGTVLALMGENGAGKSTLMKIIAGIYQPDA--GE 79
           YLLE+  I K F GV AL  + +++RPG  + L GENGAGKSTLMKI++G+Y      GE
Sbjct: 4   YLLEMKGIVKSFGGVRALNGIDIKIRPGECVGLCGENGAGKSTLMKILSGVYPHGTWEGE 63

Query: 80  IRLRGKPIVFETPLAAQKAGIAMIHQELNLMPHMSIAENIWIGREQLNSLHMVNHREMHR 139
           I   GKP+   +    + AGI +IHQEL L+P +S+AENI++G E       +N+  M+R
Sbjct: 64  ILWDGKPLQAHSVRDTEAAGIVIIHQELMLVPELSVAENIFMGHEITLPGGRMNYPAMYR 123

Query: 140 CTAELLARLRI-NLDPEEQVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITEKEVAH 198
              EL+  L + +++    V       +Q+VEIAKA++ D+ +LI+DEP+S++T  E+  
Sbjct: 124 RAEELMRELNMPDINVALPVSQYGGGHQQLVEIAKALNKDARLLILDEPSSSLTASEIGV 183

Query: 199 LFSIIADLKSQGKGIVYITHKMNEVFAIADEVAVFRDGHYIGLQRADSMNSDSLISMMVG 258
           L  II DLK++G   VYI+HK++EV  + D ++V RDG +I       M+ D +I+ MVG
Sbjct: 184 LLKIIKDLKARGVACVYISHKLDEVAEVCDTISVIRDGKHIATTPMQEMDVDKIITQMVG 243

Query: 259 RELSQLFPLRETPIGDLLLTVRDLTLDGV-------FKDVSFDLHAGEILGIAGLMGSGR 311
           RE++ ++P R   IG+++L  R++T   +         DVSF +  GEILGIAGL+G+GR
Sbjct: 244 REITAMYPERNHAIGEVVLEARNITCYDIDNPRRKRVDDVSFSVRRGEILGIAGLVGAGR 303

Query: 312 TNVAETIFGITPSS-SGQITLDGKAVRISDPHMAIEKGFALLTEDRKLSGLFPCLSVLEN 370
           T +   IFG       GQ+ L+GK    S P  +I +G  ++ EDRK  G+ P L V +N
Sbjct: 304 TELVSAIFGAYRGRYEGQVLLEGKPADTSSPLKSIRRGLCMVPEDRKHHGIVPDLDVGQN 363

Query: 371 MEMAVLPHYTGNGFIQQKALRALCEDMCKKLRVKTPSLEQCIDTLSGGNQQKALLARWLM 430
           + + VL  ++    I   A     +D   ++RVKT +    I +LSGGNQQKA+LA+ L+
Sbjct: 364 ITLTVLNRFSRGSRIDGSAELKTIQDEIGRMRVKTATPFLPITSLSGGNQQKAVLAKMLL 423

Query: 431 TNPRLLILDEPTRGIDVGAKAEIYRLIAFLASEGMAVIMISSELPEVLGMSDRVMVMHEG 490
             P++LILDEPTRG+DVGAKAEIYRLI+ LA  G+A+IM+SSEL EVLG+SDRV+V+ EG
Sbjct: 424 AQPKVLILDEPTRGVDVGAKAEIYRLISELAKAGLAIIMVSSELAEVLGVSDRVLVIGEG 483

Query: 491 ELMGTLDRSEATQEKVMQLA 510
            L G       +QE V+  A
Sbjct: 484 RLRGDFVNDNLSQETVLAAA 503



 Score = 87.8 bits (216), Expect = 9e-22
 Identities = 60/237 (25%), Positives = 118/237 (49%), Gaps = 16/237 (6%)

Query: 41  DVQLRVRPGTVLALMGENGAGKSTLMKIIAGIYQPD-AGEIRLRGKPIVFETPLAAQKAG 99
           DV   VR G +L + G  GAG++ L+  I G Y+    G++ L GKP    +PL + + G
Sbjct: 282 DVSFSVRRGEILGIAGLVGAGRTELVSAIFGAYRGRYEGQVLLEGKPADTSSPLKSIRRG 341

Query: 100 IAMIHQELN---LMPHMSIAENIWIGREQLNSLHMVNHREMHRCTAEL------LARLRI 150
           + M+ ++     ++P + + +NI      L  L+  +       +AEL      + R+R+
Sbjct: 342 LCMVPEDRKHHGIVPDLDVGQNI-----TLTVLNRFSRGSRIDGSAELKTIQDEIGRMRV 396

Query: 151 NL-DPEEQVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITEKEVAHLFSIIADLKSQ 209
               P   + +LS   +Q   +AK +     +LI+DEPT  +     A ++ +I++L   
Sbjct: 397 KTATPFLPITSLSGGNQQKAVLAKMLLAQPKVLILDEPTRGVDVGAKAEIYRLISELAKA 456

Query: 210 GKGIVYITHKMNEVFAIADEVAVFRDGHYIGLQRADSMNSDSLISMMVGRELSQLFP 266
           G  I+ ++ ++ EV  ++D V V  +G   G    D+++ +++++  + + + Q  P
Sbjct: 457 GLAIIMVSSELAEVLGVSDRVLVIGEGRLRGDFVNDNLSQETVLAAAINQPVPQATP 513


Lambda     K      H
   0.320    0.136    0.381 

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: 611
Number of extensions: 26
Number of successful extensions: 9
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 517
Length of database: 518
Length adjustment: 35
Effective length of query: 482
Effective length of database: 483
Effective search space:   232806
Effective search space used:   232806
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 (21.8 bits)
S2: 52 (24.6 bits)

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

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Protein sequences (fasta format)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources