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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AXN1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 193 | 197 | PF00656 | 0.432 |
CLV_C14_Caspase3-7 | 333 | 337 | PF00656 | 0.661 |
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 506 | 510 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.461 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.517 |
CLV_PCSK_PC7_1 | 225 | 231 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.416 |
DEG_APCC_DBOX_1 | 123 | 131 | PF00400 | 0.583 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.548 |
DEG_SCF_TRCP1_1 | 485 | 490 | PF00400 | 0.606 |
DEG_SPOP_SBC_1 | 3 | 7 | PF00917 | 0.387 |
DEG_SPOP_SBC_1 | 320 | 324 | PF00917 | 0.712 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.705 |
DEG_SPOP_SBC_1 | 497 | 501 | PF00917 | 0.621 |
DOC_CDC14_PxL_1 | 71 | 79 | PF14671 | 0.366 |
DOC_CKS1_1 | 362 | 367 | PF01111 | 0.730 |
DOC_MAPK_gen_1 | 426 | 436 | PF00069 | 0.628 |
DOC_MAPK_MEF2A_6 | 9 | 18 | PF00069 | 0.452 |
DOC_PP2B_LxvP_1 | 461 | 464 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.394 |
DOC_PP2B_PxIxI_1 | 392 | 398 | PF00149 | 0.609 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.413 |
DOC_PP4_MxPP_1 | 348 | 351 | PF00568 | 0.700 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.370 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.611 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 329 | 335 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 382 | 386 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 459 | 464 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 90 | 96 | PF00244 | 0.297 |
LIG_AP2alpha_2 | 398 | 400 | PF02296 | 0.631 |
LIG_BIR_III_2 | 279 | 283 | PF00653 | 0.578 |
LIG_EH1_1 | 81 | 89 | PF00400 | 0.391 |
LIG_EVH1_1 | 314 | 318 | PF00568 | 0.542 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.541 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.537 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.653 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.490 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.704 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.451 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.577 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.482 |
LIG_LIR_Apic_2 | 10 | 14 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 259 | 270 | PF02991 | 0.685 |
LIG_LIR_Gen_1 | 509 | 518 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 509 | 514 | PF02991 | 0.541 |
LIG_MAD2 | 47 | 55 | PF02301 | 0.485 |
LIG_MYND_1 | 389 | 393 | PF01753 | 0.636 |
LIG_SH2_NCK_1 | 262 | 266 | PF00017 | 0.610 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 182 | 185 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.375 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.621 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.644 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.648 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.545 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.679 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.559 |
LIG_SUMO_SIM_par_1 | 266 | 274 | PF11976 | 0.676 |
LIG_SUMO_SIM_par_1 | 373 | 380 | PF11976 | 0.528 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.371 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.488 |
LIG_TRAF2_1 | 413 | 416 | PF00917 | 0.657 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.427 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.517 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.655 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.539 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.536 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.661 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.540 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.612 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.656 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.591 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.592 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.432 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.408 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.374 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.489 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.580 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.403 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.482 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.467 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.650 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.459 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.349 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.559 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.572 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.705 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.574 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.665 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.719 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.516 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.632 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.357 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.403 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.553 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.685 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.664 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.485 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.701 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.608 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.605 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.615 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.612 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.616 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.610 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.769 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.376 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.524 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.410 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.352 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.405 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.400 |
MOD_NEK2_2 | 454 | 459 | PF00069 | 0.640 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.538 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.537 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.655 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.396 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.655 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.525 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.315 |
MOD_Plk_2-3 | 196 | 202 | PF00069 | 0.390 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.396 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.665 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.473 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.442 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.420 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.704 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.626 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.647 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.556 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.611 |
MOD_SUMO_for_1 | 102 | 105 | PF00179 | 0.582 |
TRG_DiLeu_BaEn_1 | 239 | 244 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 456 | 461 | PF01217 | 0.631 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.370 |
TRG_DiLeu_BaLyEn_6 | 164 | 169 | PF01217 | 0.390 |
TRG_DiLeu_LyEn_5 | 456 | 461 | PF01217 | 0.519 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.609 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.457 |
TRG_NES_CRM1_1 | 13 | 27 | PF08389 | 0.360 |
TRG_NLS_MonoExtC_3 | 425 | 430 | PF00514 | 0.703 |
TRG_NLS_MonoExtN_4 | 423 | 430 | PF00514 | 0.702 |
TRG_Pf-PMV_PEXEL_1 | 516 | 521 | PF00026 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYY1 | Leptomonas seymouri | 38% | 100% |
A0A3Q8ICE6 | Leishmania donovani | 86% | 100% |
A4HEK1 | Leishmania braziliensis | 70% | 99% |
A4I1J7 | Leishmania infantum | 86% | 100% |
Q4Q9U0 | Leishmania major | 86% | 100% |