Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate Pf1N1B4_1109 2-ketoglutaric semialdehyde dehydrogenase (EC 1.2.1.26)
Query= curated2:Q2SXN9 (487 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_1109 Length = 481 Score = 219 bits (559), Expect = 1e-61 Identities = 167/470 (35%), Positives = 228/470 (48%), Gaps = 21/470 (4%) Query: 5 FIDGAWVDGAGPVFASRNPGT-NERVWEGASASADDVERAVASARRAFAAWSALDLDARC 63 +I+G WV GA A+ NP + + + A A V A+ +AR AF AWS + AR Sbjct: 10 YINGEWVSGAD-YSANINPSELTDTIGDYAKADLAQVHAAIDAARAAFPAWSTSGIQARH 68 Query: 64 TIVKRFAALLVERKEALATMIGRETGKPLWEARTEVASMAAKVDISITAYHERTGEKRAP 123 + + ++ R+E L T++ RE GK L EA EV +G+ Sbjct: 69 DSLDKVGTEILARREELGTLLAREEGKTLPEAIGEVTRAGNIFKFFAGECLRLSGDYLPS 128 Query: 124 MADGVAV-LRHRPHGVVAVFGPYNFPGHLPNGHIVPALIAGNTVVFKPSELAPGVARATV 182 + GV V + GVV + P+NFP +P I PAL GN VV KP++L PG A A Sbjct: 129 VRPGVNVEVTREALGVVGLITPWNFPIAIPAWKIAPALAYGNCVVLKPADLVPGCAWALA 188 Query: 183 EIWRDAGLPAGVLNLVQGE-KDTGVALANHRQIDGLFFTGSSDTGTLLHKQFGGRPEIVL 241 EI AG PAGV NLV G + G AL ++DG+ FTGS G + R + + Sbjct: 189 EIISRAGFPAGVFNLVMGSGRVVGDALVQSPKVDGISFTGSVGVGRQIAVSCVSR-QAKV 247 Query: 242 ALEMGGNNPLVVAEVEDIDAAVHHAIQSAFLSAGQRCTCARRILVPRGAFGDRFVARLAD 301 LEMGG NP ++ + D+ AV ++QSAF S GQRCT + R +V G D+FV +A+ Sbjct: 248 QLEMGGKNPQIILDDADLKQAVELSVQSAFYSTGQRCTASSRFIVTAGIH-DKFVEAMAE 306 Query: 302 VASKIT---ASVFDADPQPFMGAVISARAASRLVAAQ---ARLVGLGASPIIEMKQRDPA 355 I A D P + + + Q ARLV G + + Sbjct: 307 RMKSIKVGHALKTGTDIGPVVSQAQLEQDLKYIDIGQSEGARLVSGGGLVACDTE----- 361 Query: 356 LGFVNAAIL--DVTNVRELPDEEHFGPLAQIVRYTDLDDAIARANDTAFGLSAGLLADDE 413 G+ A L D T + EE FGP+A IVR D + A+A ANDT FGLSAG+ Sbjct: 362 -GYFLAPTLFADSTAAMRISREEIFGPVANIVRVADYEAALAMANDTEFGLSAGIATTSL 420 Query: 414 QAWHTFRRAIRAGIVNWNRPTNGASSAAPFGG-AGRSGNHRPSAYYAADY 462 + + F+R +AG+V N PT G PFGG G S R YA ++ Sbjct: 421 KYANHFKRHSQAGMVMVNLPTAGVDYHVPFGGRKGSSYGSREQGRYAQEF 470 Lambda K H 0.320 0.134 0.402 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: 501 Number of extensions: 22 Number of successful extensions: 4 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: 487 Length of database: 481 Length adjustment: 34 Effective length of query: 453 Effective length of database: 447 Effective search space: 202491 Effective search space used: 202491 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 Apr 09 2024. The underlying query database was built on Sep 17 2021.
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