Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 9 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 18 |
GO:0016020 | membrane | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A4H9Y5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006897 | endocytosis | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0016197 | endosomal transport | 4 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 18 |
GO:0005488 | binding | 1 | 18 |
GO:0005525 | GTP binding | 5 | 18 |
GO:0017076 | purine nucleotide binding | 4 | 18 |
GO:0019001 | guanyl nucleotide binding | 5 | 18 |
GO:0032553 | ribonucleotide binding | 3 | 18 |
GO:0032555 | purine ribonucleotide binding | 4 | 18 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 18 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 18 |
GO:0036094 | small molecule binding | 2 | 18 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043168 | anion binding | 3 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:0097367 | carbohydrate derivative binding | 2 | 18 |
GO:1901265 | nucleoside phosphate binding | 3 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.188 |
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.318 |
CLV_C14_Caspase3-7 | 448 | 452 | PF00656 | 0.664 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.461 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 335 | 337 | PF00082 | 0.203 |
CLV_PCSK_PC1ET2_1 | 454 | 456 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.343 |
CLV_Separin_Metazoa | 234 | 238 | PF03568 | 0.376 |
CLV_Separin_Metazoa | 254 | 258 | PF03568 | 0.387 |
DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.276 |
DEG_APCC_DBOX_1 | 321 | 329 | PF00400 | 0.330 |
DEG_APCC_DBOX_1 | 421 | 429 | PF00400 | 0.348 |
DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.622 |
DEG_SPOP_SBC_1 | 565 | 569 | PF00917 | 0.521 |
DOC_CYCLIN_RxL_1 | 123 | 135 | PF00134 | 0.409 |
DOC_CYCLIN_yCln2_LP_2 | 70 | 76 | PF00134 | 0.285 |
DOC_MAPK_gen_1 | 172 | 179 | PF00069 | 0.339 |
DOC_MAPK_gen_1 | 306 | 313 | PF00069 | 0.314 |
DOC_MAPK_MEF2A_6 | 186 | 194 | PF00069 | 0.251 |
DOC_MAPK_NFAT4_5 | 186 | 194 | PF00069 | 0.188 |
DOC_PP2B_LxvP_1 | 594 | 597 | PF13499 | 0.567 |
DOC_PP2B_LxvP_1 | 603 | 606 | PF13499 | 0.541 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.354 |
DOC_PP4_FxxP_1 | 193 | 196 | PF00568 | 0.285 |
DOC_PP4_FxxP_1 | 497 | 500 | PF00568 | 0.784 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.276 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.681 |
DOC_USP7_UBL2_3 | 331 | 335 | PF12436 | 0.317 |
DOC_USP7_UBL2_3 | 382 | 386 | PF12436 | 0.404 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.502 |
LIG_14-3-3_CanoR_1 | 153 | 157 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 564 | 570 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 65 | 71 | PF00244 | 0.371 |
LIG_Actin_WH2_2 | 209 | 227 | PF00022 | 0.250 |
LIG_Actin_WH2_2 | 390 | 408 | PF00022 | 0.371 |
LIG_APCC_ABBA_1 | 190 | 195 | PF00400 | 0.285 |
LIG_APCC_ABBA_1 | 426 | 431 | PF00400 | 0.552 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.376 |
LIG_BRCT_BRCA1_1 | 478 | 482 | PF00533 | 0.505 |
LIG_BRCT_BRCA1_1 | 493 | 497 | PF00533 | 0.562 |
LIG_Clathr_ClatBox_1 | 191 | 195 | PF01394 | 0.188 |
LIG_CtBP_PxDLS_1 | 500 | 504 | PF00389 | 0.504 |
LIG_EH_1 | 414 | 418 | PF12763 | 0.630 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.358 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.458 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.435 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.276 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.540 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.262 |
LIG_FXI_DFP_1 | 357 | 361 | PF00024 | 0.276 |
LIG_LIR_Apic_2 | 262 | 267 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 494 | 500 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 175 | 184 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 270 | 278 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 64 | 73 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 99 | 107 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 376 | 381 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.298 |
LIG_Pex14_1 | 264 | 268 | PF04695 | 0.411 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.305 |
LIG_Pex14_2 | 209 | 213 | PF04695 | 0.262 |
LIG_Pex14_2 | 273 | 277 | PF04695 | 0.368 |
LIG_Pex14_2 | 369 | 373 | PF04695 | 0.266 |
LIG_Pex14_2 | 52 | 56 | PF04695 | 0.318 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.288 |
LIG_PTB_Apo_2 | 118 | 125 | PF02174 | 0.188 |
LIG_PTB_Phospho_1 | 118 | 124 | PF10480 | 0.188 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.318 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.364 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.347 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.334 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.365 |
LIG_SH2_STAT3 | 84 | 87 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.197 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.317 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.689 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.693 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.658 |
LIG_SUMO_SIM_anti_2 | 152 | 159 | PF11976 | 0.321 |
LIG_SUMO_SIM_anti_2 | 187 | 193 | PF11976 | 0.188 |
LIG_SUMO_SIM_anti_2 | 279 | 287 | PF11976 | 0.431 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.509 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.409 |
LIG_TRAF2_1 | 584 | 587 | PF00917 | 0.607 |
LIG_TRAF2_2 | 293 | 298 | PF00917 | 0.378 |
LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.374 |
LIG_WW_3 | 254 | 258 | PF00397 | 0.387 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.538 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.610 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.580 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.454 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.384 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.494 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.287 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.734 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.262 |
MOD_Cter_Amidation | 438 | 441 | PF01082 | 0.431 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.653 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.383 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.593 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.751 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.727 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.576 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.636 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.305 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.336 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.377 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.717 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.552 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.602 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.494 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.655 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.723 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.736 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.661 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.319 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.319 |
MOD_LATS_1 | 562 | 568 | PF00433 | 0.519 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.386 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.407 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.388 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.307 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.356 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.337 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.482 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.623 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.795 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.490 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.417 |
MOD_NEK2_2 | 66 | 71 | PF00069 | 0.276 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.360 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.285 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.382 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.716 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.318 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.318 |
MOD_PKB_1 | 430 | 438 | PF00069 | 0.354 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.263 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.358 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.747 |
MOD_Plk_2-3 | 146 | 152 | PF00069 | 0.406 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.296 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.338 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.381 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.375 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.380 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.318 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.324 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.591 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.327 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.499 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.698 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.281 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.340 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.305 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.535 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.723 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.758 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.718 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.608 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.502 |
MOD_SUMO_rev_2 | 274 | 282 | PF00179 | 0.480 |
TRG_DiLeu_BaEn_1 | 146 | 151 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_1 | 185 | 190 | PF01217 | 0.318 |
TRG_DiLeu_BaEn_1 | 280 | 285 | PF01217 | 0.354 |
TRG_DiLeu_BaEn_1 | 385 | 390 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_1 | 421 | 426 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.158 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.480 |
TRG_NLS_Bipartite_1 | 440 | 458 | PF00514 | 0.466 |
TRG_NLS_MonoExtC_3 | 334 | 340 | PF00514 | 0.294 |
TRG_NLS_MonoExtN_4 | 333 | 339 | PF00514 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 432 | 436 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8K7 | Leptomonas seymouri | 74% | 100% |
A0A0S4KGM0 | Bodo saltans | 64% | 100% |
A0A1X0P6D7 | Trypanosomatidae | 61% | 100% |
A0A3R7LDF3 | Trypanosoma rangeli | 60% | 100% |
A0A3S7WV81 | Leishmania donovani | 75% | 99% |
A0A3S7X801 | Leishmania donovani | 46% | 100% |
A0A422P0G8 | Trypanosoma rangeli | 46% | 100% |
A4HAT9 | Leishmania braziliensis | 44% | 100% |
A4HY50 | Leishmania infantum | 75% | 99% |
A4IA07 | Leishmania infantum | 46% | 100% |
D0A0F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9ARX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
E9B513 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
Q4Q2X3 | Leishmania major | 47% | 100% |
Q4QDJ3 | Leishmania major | 75% | 100% |
V5BSA9 | Trypanosoma cruzi | 59% | 100% |