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: E9ARL2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.491 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.676 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.779 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.560 |
CLV_PCSK_PC7_1 | 136 | 142 | PF00082 | 0.548 |
CLV_PCSK_PC7_1 | 184 | 190 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.769 |
DEG_SPOP_SBC_1 | 60 | 64 | PF00917 | 0.676 |
DOC_CKS1_1 | 177 | 182 | PF01111 | 0.528 |
DOC_MAPK_gen_1 | 140 | 149 | PF00069 | 0.683 |
DOC_MAPK_gen_1 | 33 | 41 | PF00069 | 0.612 |
DOC_MAPK_MEF2A_6 | 140 | 149 | PF00069 | 0.722 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.556 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.690 |
DOC_PP4_FxxP_1 | 472 | 475 | PF00568 | 0.717 |
DOC_PP4_FxxP_1 | 482 | 485 | PF00568 | 0.628 |
DOC_PP4_FxxP_1 | 491 | 494 | PF00568 | 0.603 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.821 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.818 |
LIG_14-3-3_CanoR_1 | 105 | 113 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 141 | 145 | PF00244 | 0.826 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 266 | 272 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 309 | 316 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 469 | 475 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 536 | 542 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 65 | 72 | PF00244 | 0.644 |
LIG_Actin_WH2_2 | 251 | 268 | PF00022 | 0.453 |
LIG_APCC_Cbox_1 | 240 | 246 | PF00515 | 0.461 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.717 |
LIG_BIR_III_4 | 318 | 322 | PF00653 | 0.686 |
LIG_CaM_NSCaTE_8 | 326 | 333 | PF13499 | 0.324 |
LIG_deltaCOP1_diTrp_1 | 358 | 366 | PF00928 | 0.481 |
LIG_deltaCOP1_diTrp_1 | 456 | 466 | PF00928 | 0.676 |
LIG_EH1_1 | 47 | 55 | PF00400 | 0.710 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.748 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.657 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.537 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.557 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.598 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.654 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.642 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.480 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.500 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.666 |
LIG_FXI_DFP_1 | 463 | 467 | PF00024 | 0.682 |
LIG_LIR_Apic_2 | 379 | 383 | PF02991 | 0.688 |
LIG_LIR_Apic_2 | 479 | 485 | PF02991 | 0.606 |
LIG_LIR_Apic_2 | 489 | 494 | PF02991 | 0.637 |
LIG_LIR_Apic_2 | 529 | 534 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 150 | 159 | PF02991 | 0.690 |
LIG_LIR_Gen_1 | 337 | 346 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 358 | 369 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 476 | 485 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.757 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 323 | 329 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 337 | 342 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 379 | 384 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 476 | 481 | PF02991 | 0.662 |
LIG_NRBOX | 203 | 209 | PF00104 | 0.624 |
LIG_NRBOX | 283 | 289 | PF00104 | 0.546 |
LIG_NRBOX | 5 | 11 | PF00104 | 0.485 |
LIG_PDZ_Class_1 | 537 | 542 | PF00595 | 0.710 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.767 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.403 |
LIG_SH2_SRC | 272 | 275 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 478 | 482 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.768 |
LIG_SH3_1 | 142 | 148 | PF00018 | 0.730 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.730 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.648 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.721 |
LIG_SUMO_SIM_anti_2 | 198 | 206 | PF11976 | 0.624 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.635 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.570 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.610 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.706 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.372 |
LIG_TRAF2_1 | 29 | 32 | PF00917 | 0.586 |
LIG_TRAF2_1 | 517 | 520 | PF00917 | 0.713 |
LIG_UBA3_1 | 254 | 260 | PF00899 | 0.517 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.739 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.600 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.684 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.699 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.594 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.658 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.450 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.753 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.687 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.742 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.651 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.553 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.362 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.567 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.726 |
MOD_Cter_Amidation | 138 | 141 | PF01082 | 0.545 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.684 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.704 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.703 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.578 |
MOD_GlcNHglycan | 318 | 322 | PF01048 | 0.760 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.727 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.796 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.687 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.687 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.664 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.745 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.711 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.708 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.471 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.607 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.570 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.497 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.781 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.689 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.620 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.734 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.752 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.525 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.627 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.501 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.474 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.531 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.614 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.623 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.733 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.706 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.716 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.630 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.506 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.725 |
MOD_PKA_1 | 140 | 146 | PF00069 | 0.641 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.687 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.634 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.663 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.688 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.716 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.630 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.506 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.738 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.489 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.711 |
MOD_Plk_2-3 | 161 | 167 | PF00069 | 0.663 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.765 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.640 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.596 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.420 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.546 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.548 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.520 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.673 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.667 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.653 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.433 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.572 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.796 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.622 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.741 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.525 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.728 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.704 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.718 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.821 |
MOD_SUMO_for_1 | 517 | 520 | PF00179 | 0.713 |
TRG_DiLeu_LyEn_5 | 293 | 298 | PF01217 | 0.584 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.684 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.663 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.723 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.735 |
TRG_ER_diArg_1 | 468 | 470 | PF00400 | 0.782 |
TRG_ER_diArg_1 | 536 | 539 | PF00400 | 0.679 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.751 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2K4 | Leptomonas seymouri | 38% | 100% |
A0A3Q8IE86 | Leishmania donovani | 84% | 99% |
A4H9I6 | Leishmania braziliensis | 57% | 97% |
A4HXU9 | Leishmania infantum | 83% | 100% |
Q4QDW7 | Leishmania major | 79% | 100% |