Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005778 | peroxisomal membrane | 6 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031903 | microbody membrane | 5 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: Q4QAW3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0051301 | cell division | 2 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006625 | protein targeting to peroxisome | 5 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007031 | peroxisome organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0043574 | peroxisomal transport | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072662 | protein localization to peroxisome | 6 | 1 |
GO:0072663 | establishment of protein localization to peroxisome | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0016462 | pyrophosphatase activity | 5 | 15 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 15 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 15 |
GO:0016887 | ATP hydrolysis activity | 7 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 15 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004176 | ATP-dependent peptidase activity | 2 | 1 |
GO:0004222 | metalloendopeptidase activity | 5 | 1 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008237 | metallopeptidase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.593 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.379 |
DEG_APCC_DBOX_1 | 176 | 184 | PF00400 | 0.573 |
DEG_APCC_DBOX_1 | 389 | 397 | PF00400 | 0.382 |
DEG_SPOP_SBC_1 | 135 | 139 | PF00917 | 0.395 |
DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.551 |
DOC_CDC14_PxL_1 | 434 | 442 | PF14671 | 0.326 |
DOC_CYCLIN_yCln2_LP_2 | 100 | 106 | PF00134 | 0.368 |
DOC_CYCLIN_yCln2_LP_2 | 62 | 68 | PF00134 | 0.550 |
DOC_MAPK_DCC_7 | 348 | 356 | PF00069 | 0.209 |
DOC_MAPK_gen_1 | 262 | 271 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 348 | 357 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 427 | 437 | PF00069 | 0.277 |
DOC_MAPK_gen_1 | 463 | 470 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 348 | 356 | PF00069 | 0.266 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.377 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.548 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.506 |
DOC_USP7_UBL2_3 | 30 | 34 | PF12436 | 0.443 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 264 | 269 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 309 | 315 | PF00244 | 0.349 |
LIG_Actin_WH2_2 | 326 | 343 | PF00022 | 0.306 |
LIG_Actin_WH2_2 | 482 | 498 | PF00022 | 0.513 |
LIG_Actin_WH2_2 | 512 | 529 | PF00022 | 0.512 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.455 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.385 |
LIG_deltaCOP1_diTrp_1 | 446 | 453 | PF00928 | 0.359 |
LIG_EH1_1 | 262 | 270 | PF00400 | 0.507 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.389 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.460 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.367 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.255 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.528 |
LIG_Integrin_RGD_1 | 372 | 374 | PF01839 | 0.190 |
LIG_LIR_Apic_2 | 433 | 439 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 21 | 27 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 314 | 323 | PF02991 | 0.225 |
LIG_LIR_Gen_1 | 450 | 460 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.506 |
LIG_MYND_1 | 163 | 167 | PF01753 | 0.407 |
LIG_MYND_1 | 99 | 103 | PF01753 | 0.377 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.395 |
LIG_NRBOX | 127 | 133 | PF00104 | 0.467 |
LIG_NRBOX | 392 | 398 | PF00104 | 0.277 |
LIG_PCNA_yPIPBox_3 | 427 | 435 | PF02747 | 0.425 |
LIG_PCNA_yPIPBox_3 | 483 | 496 | PF02747 | 0.499 |
LIG_Pex14_1 | 448 | 452 | PF04695 | 0.359 |
LIG_Pex14_1 | 77 | 81 | PF04695 | 0.406 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.398 |
LIG_REV1ctd_RIR_1 | 450 | 459 | PF16727 | 0.449 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.481 |
LIG_SH2_NCK_1 | 81 | 85 | PF00017 | 0.413 |
LIG_SH2_PTP2 | 436 | 439 | PF00017 | 0.326 |
LIG_SH2_SRC | 436 | 439 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.395 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.629 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.326 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.461 |
LIG_SUMO_SIM_anti_2 | 110 | 116 | PF11976 | 0.394 |
LIG_SUMO_SIM_anti_2 | 358 | 364 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 353 | 359 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 465 | 472 | PF11976 | 0.487 |
LIG_TYR_ITIM | 79 | 84 | PF00017 | 0.479 |
LIG_UBA3_1 | 22 | 30 | PF00899 | 0.392 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.433 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.410 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.536 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.494 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.474 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.559 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.636 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.529 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.439 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.629 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.279 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.383 |
MOD_GlcNHglycan | 405 | 409 | PF01048 | 0.348 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.473 |
MOD_GlcNHglycan | 491 | 495 | PF01048 | 0.474 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.508 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.522 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.541 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.434 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.496 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.406 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.473 |
MOD_LATS_1 | 241 | 247 | PF00433 | 0.668 |
MOD_N-GLC_2 | 211 | 213 | PF02516 | 0.534 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.414 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.415 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.561 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.573 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.611 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.587 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.277 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.340 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.463 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.447 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.404 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.413 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.410 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.255 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.504 |
MOD_PK_1 | 102 | 108 | PF00069 | 0.382 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.408 |
MOD_PKB_1 | 262 | 270 | PF00069 | 0.507 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.504 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.459 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.326 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.468 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.464 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.404 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.540 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.398 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.370 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.306 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.394 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.430 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.693 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.614 |
TRG_DiLeu_BaEn_2 | 18 | 24 | PF01217 | 0.338 |
TRG_DiLeu_BaEn_2 | 233 | 239 | PF01217 | 0.641 |
TRG_DiLeu_BaLyEn_6 | 123 | 128 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 96 | 101 | PF01217 | 0.419 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 348 | 351 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 526 | 528 | PF00400 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 15 | 19 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 331 | 335 | PF00026 | 0.320 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTJ8 | Leptomonas seymouri | 63% | 100% |
A0A0S4IKL1 | Bodo saltans | 28% | 80% |
A0A0S4J3P5 | Bodo saltans | 32% | 100% |
A0A1X0NKH8 | Trypanosomatidae | 36% | 100% |
A0A1X0NXH5 | Trypanosomatidae | 25% | 75% |
A0A3Q8IG04 | Leishmania donovani | 93% | 100% |
A0A3R7MBQ6 | Trypanosoma rangeli | 38% | 100% |
A4HD75 | Leishmania braziliensis | 83% | 95% |
D0A6Y7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 99% |
E9AH29 | Leishmania infantum | 93% | 100% |
E9AWK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5B4C8 | Trypanosoma cruzi | 26% | 93% |
V5BRB9 | Trypanosoma cruzi | 40% | 100% |