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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 9 |
GO:0032991 | protein-containing complex | 1 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043228 | non-membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:1990904 | ribonucleoprotein complex | 2 | 9 |
Related structures:
AlphaFold database: Q4Q954
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0008270 | zinc ion binding | 6 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0046914 | transition metal ion binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.606 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.666 |
DEG_SPOP_SBC_1 | 26 | 30 | PF00917 | 0.556 |
DEG_SPOP_SBC_1 | 328 | 332 | PF00917 | 0.610 |
DOC_ANK_TNKS_1 | 323 | 330 | PF00023 | 0.488 |
DOC_ANK_TNKS_1 | 357 | 364 | PF00023 | 0.486 |
DOC_MAPK_gen_1 | 154 | 162 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 64 | 71 | PF00069 | 0.647 |
DOC_MAPK_RevD_3 | 141 | 156 | PF00069 | 0.558 |
DOC_PP4_FxxP_1 | 457 | 460 | PF00568 | 0.475 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.785 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.478 |
DOC_USP7_MATH_2 | 78 | 84 | PF00917 | 0.648 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.482 |
LIG_14-3-3_CanoR_1 | 146 | 152 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 156 | 161 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 24 | 34 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 411 | 415 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 448 | 454 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 491 | 500 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 517 | 527 | PF00244 | 0.426 |
LIG_AP2alpha_2 | 217 | 219 | PF02296 | 0.447 |
LIG_BIR_III_4 | 245 | 249 | PF00653 | 0.551 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.473 |
LIG_deltaCOP1_diTrp_1 | 466 | 476 | PF00928 | 0.539 |
LIG_eIF4E_1 | 379 | 385 | PF01652 | 0.531 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.461 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.423 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.618 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.562 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.555 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.442 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.437 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.463 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.492 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.482 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.708 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.681 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.566 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.517 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.419 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.530 |
LIG_LIR_Apic_2 | 197 | 201 | PF02991 | 0.675 |
LIG_LIR_Apic_2 | 323 | 328 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 525 | 531 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 574 | 581 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 126 | 130 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.518 |
LIG_LYPXL_yS_3 | 179 | 182 | PF13949 | 0.510 |
LIG_MAD2 | 498 | 506 | PF02301 | 0.324 |
LIG_NRBOX | 208 | 214 | PF00104 | 0.450 |
LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.639 |
LIG_SH2_NCK_1 | 325 | 329 | PF00017 | 0.562 |
LIG_SH2_SRC | 360 | 363 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.496 |
LIG_SH2_STAT3 | 512 | 515 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.497 |
LIG_SH3_1 | 424 | 430 | PF00018 | 0.530 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.582 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.452 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.669 |
LIG_Sin3_3 | 290 | 297 | PF02671 | 0.503 |
LIG_SUMO_SIM_par_1 | 93 | 99 | PF11976 | 0.561 |
LIG_TRFH_1 | 421 | 425 | PF08558 | 0.450 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.676 |
MOD_CDK_SPxxK_3 | 510 | 517 | PF00069 | 0.483 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.679 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.538 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.516 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.437 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.446 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.650 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.759 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.504 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.484 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.314 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.608 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.469 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.752 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.747 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.594 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.435 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.484 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.524 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.452 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.382 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.517 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.499 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.370 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.501 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.507 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.445 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.390 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.430 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.471 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.451 |
MOD_NEK2_2 | 506 | 511 | PF00069 | 0.474 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.722 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.539 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.529 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.465 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.496 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.495 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.506 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.455 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.495 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.464 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.643 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.505 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.577 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.475 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.515 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.457 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.474 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.737 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.479 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.457 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.682 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.480 |
MOD_SUMO_rev_2 | 200 | 209 | PF00179 | 0.670 |
MOD_SUMO_rev_2 | 438 | 442 | PF00179 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 71 | 76 | PF01217 | 0.725 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.510 |
TRG_ER_diArg_1 | 550 | 553 | PF00400 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 462 | 466 | PF00026 | 0.339 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUB1 | Leptomonas seymouri | 63% | 100% |
A0A0S4KLR3 | Bodo saltans | 26% | 100% |
A0A1X0NS60 | Trypanosomatidae | 32% | 100% |
A0A3S7WZV3 | Leishmania donovani | 93% | 100% |
A0A422NIT0 | Trypanosoma rangeli | 37% | 100% |
A4HEZ5 | Leishmania braziliensis | 74% | 99% |
A4I269 | Leishmania infantum | 93% | 100% |
C4Q0P6 | Schistosoma mansoni | 23% | 100% |
C9ZRS8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AYB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
V5BEB9 | Trypanosoma cruzi | 34% | 100% |